Chemotherapy in conjoint aging-tumor systems: some simple models for addressing coupled aging-cancer dynamics
© Feizabadi and Witten; licensee BioMed Central Ltd. 2010
Received: 2 March 2010
Accepted: 15 June 2010
Published: 15 June 2010
In this paper we consider two approaches to examining the complex dynamics of conjoint aging-cancer cellular systems undergoing chemotherapeutic intervention. In particular, we focus on the effect of cells growing conjointly in a culture plate as a precursor to considering the larger multi-dimensional models of such systems. Tumor cell growth is considered from both the logistic and the Gompertzian case, while normal cell growth of fibroblasts (WI-38 human diploid fibroblasts) is considered as logistic only.
We demonstrate, in a simple approach, how the interdependency of different cell types in a tumor, together with specifications of for treatment, can lead to different evolutionary patterns for normal and tumor cells during a course of therapy.
These results have significance for understanding appropriate pharmacotherapy for elderly patients who are also undergoing chemotherapy.
In 1976 I (TMW) attended a small meeting at the W. Alton Jones Cell Science Center, a research center in upstate New York. I was a young graduate student and one of the presenters was a then very young James Smith. He presented a talk on WI-38 human diploid fibroblast doubling and aging . The results of his work lead to clonal fibroblast data distributions that looked surprisingly similar to my Master's degree modeling work on recombination of tandem gene repeats and their possible relationship to aging and cancer [2, 3]. I was immediately addicted to trying to model the processes of aging in normal cells. Not that long afterwards, I attended a cancer conference and two presenters, Leonard Weiss and Robert Kerbel, grabbed my attention talking about cancer metastasis. For me, now intrigued by biomedical aging processes, the obvious question was "how does aging change metastasic processes?" Despite what I thought were some rather elegantly designed experiments put forth in grant proposals designed to study this question in mice, the American Cancer Society felt that the topic was not relevant and that I - a mathematical physicist - was far from qualified to perform said proposed experiments. They were quite correct on the latter and far from correct on the former.
Despite my initial failures with the ACS grants, I felt quite committed to trying to develop a mathematical model of normally aging fibroblast cells. Models of cancer cells and cancer cell population behavior abounded, but nowhere could I find a model that described cellular aging [4, 5]. Thus began a decade of research papers [6–9] culminating in a series of cellular aging modeling developments [10, 11] that were eventually laid to rest due to lack of ability to obtain the experimental data needed to expand and validate the models. In parallel, I also developed a series of models attempting to describe the interplay of aging normal fibroblasts and tumor cells [6, 12–14].
Not long after the retirement of this research effort, I was asked to contribute to a special issue of the Journal of Gerontology on the subject of aging and cancer. That paper, Witten (1986)  presented the first simple ordinary differential equation model of conjoint tumor-normal cell growth, demonstrating that it was - in fact - possible to obtain different joint cellular stability configurations for the two cell populations, depending upon how the cells talked with each other through the set of rules defining inter-cellular communication. We begin by asking the following question: Why study the aging-cancer question?
The Aging-Cancer Question
Demographics of Aging
In the United States, more than 13 percent of the total population is over the age of 65, representing one in every eight Americans . The majority of these older people are women, representing almost 60 percent of the elderly population . More than half of this population falls in Hooyman & Kiyak's classification of young old; 53 percent are between 65 and 74 years of age. While the oldest old (85 years old and over) represent only 12% of this group, this is the fastest-growing demographic group in the United States . People of ethnic minority status represented only 16 percent of the elderly population in 1998, yet this is rapidly changing. By the year 2050, more than 30 percent of the older Americans will be those who are not primarily of European ancestry, including 16 percent Hispanics, 10 percent African Americans, 7 percent Asian and Pacific Islanders, and 1 percent Native Americans, according to current estimates .
Poverty is a major concern for all older Americans, particularly in the light of recent increases in the cost of health care, including medications. Lack of comprehensive health care contributes to increased levels of poverty among the old. More than half of elderly persons report living with at least one disability. The poverty rate is doubled among those whose disability affects their mobility or their ability to take care of themselves . The implication here is that many of these individuals cannot afford their own medications much less treatment for cancer.
Based on the federal poverty guidelines, 11 percent of the old live in poverty, with another 6 percent living near poverty levels, with incomes just 25 percent higher than the poverty line . Twenty-six percent of African American and 21 percent of Hispanic elderly persons live in poverty . These figures may not offer a complete picture of the socioeconomic state for most of the old in the United States. AARP states that 40 percent of all older people in the United States live on incomes less than 200 percent of the poverty level .
Nearly twice as many older women than older men live in poverty: 13 percent versus 7 percent. Older members of minority groups and those who live alone also experience a higher risk of poverty [15, 16]. Twenty percent of older persons who live alone are poor. Almost half of old women (42%) live alone, as opposed to old men (20%), resulting in higher poverty rates among women. This discrepancy is more pronounced among members of many ethnic minorities, because the life expectancy of men is proportionately lower . Thirteen percent of white (European American) women who live alone live in poverty. Almost half (49%) of African American women who live alone are living below the poverty level . It is estimated that without Social Security, the elderly poverty rate would soar to 54 percent [15, 16].
The preceding portion of this discussion has focused on Western nations, while including some salient facts about global aging [17–29]. In 2000, there were 600 million people aged 60 and over in the world . The World Health Organization estimates that there will be 1.2 billion people aged 60 and over by 2025 and 2 billion by 2050. Today, about 66% of all older people are living in the developing world; by 2025 it will be 75%. As of 1 July 2004, there were 36.3 million people in the US, over the age of 65, 4.8 million people over the age of 85, and 64,658 people estimated to be 100 years old or over on 1 August 2004. It is projected that there will be 86.7 million people in the US, over the age of 65 in the year 2050, comprising 21% of the total US population at that time. This will represent a 147% increase in the 65 years old and over population in the United States between 2004 and 2050.
In terms of percent of population aged 65 and over, the US is young in comparison to the rest of the developed world. With the exception of Japan, the world's 25 oldest countries (as of 2001) are all in Europe (see Figure 2, 3 of . Projections of the monthly gain of individuals age 65 and over, to the year 2010, are as large as 847,000 people per month worldwide. In 2000, 615,000 of the world's net gain of elderly individuals per month occurred in developing countries . Projections for Europe indicate that by 2015, the percentage of over 65-year old individuals will be the greatest and by 2030, nearly 12% of all Europeans are projected to be over the age of 74 and 7% are projected to be over the age of 79. Levels in Asia, Latin America/Caribbean are expected to more than double by 2030, while aggregate proportions of elderly in the Sub-Saharan Africa are projected to grow modestly as a result of continued high fertility in many nations . However, in the developed world, the very old (ages 80 and older) is the fastest growing population sub-component . Given these trends, late life and end of life care will become increasingly important in the decades ahead . As part of this lifecare, cancer therapy will become a more and more important component as the global population continues to age.
Demographics of Aging and Cancer
In 1974 Burnet  published data which illustrated an age-specific exponential increase in certain human cancers; stomach cancer in males, breast cancer in females. Pitot  also addressed aging and carcinogenesis. His Table  provides an excellent comparison between neoplasia and aging factors; reinforcing the variety of similarities between the two processes. In 1981, Cohen et al. show much the same results for the incidence of hematologic tumors in humans. A 1982 Oncology Overview  cites 192 abstracts of papers discussing the age-related factors which may predispose to carcinogenesis. In that same year Weindruch & Walford  pointed out that lifelong dietary restriction, beginning at 3-6 weeks of age in rodents is known to decelerate the rate of aging, increase mean and maximum lifespans and to inhibit the occurrence of many spontaneous tumors. DeVita  contains some 33 papers discussing issues that impinge on the age-related incidence of various types of cancer. Ebbesen  discusses the probable mechanisms of cancer development and "those aspects of 'normal' aging that he believes to be most relevant to the etiologic and pathogenetic bonds between the two biological processes." These mechanisms are explored in Macieria-Coelho & Azzarone . Mathe & Reizenstein  further discuss the aging-cancer relationship in humans. They point out that incidence of many tumors (most of the carcinomas and leukemias) increases with age; for a combination of reasons. Among these reasons are environmental factors, decreased DNA repair function, decreased immunological and biological surveillance for tumors, and a lack of hormonal regulation. The incidence rates are seen to rise sharply, once one is past the age of thirty, with a dramatic increase once one is past the age of fifty.
Cellular Aging and Cancer
Age-related Cancer Treatment
As we age, our bodies change in numerous ways. Biomedical dynamics is altered, metabolism slows, organ function can diminish in conjunction with an increase in the number of prescription drugs taken. Liver and kidney function can change making clearance rates for drugs change and potentially increasing the chances of multi-drug interactions that could be harmful or even fatal. The body's ability to withstand toxins  often decreases making it potentially more difficult to treat various forms of cancer with cytotoxic agents [44–46]. Pharmacological considerations must also be taken into account, not only from the perspective of which is the optimal chemotherapeutic agent and at what toxicity level, but also one must consider what other drugs the patient is taking and how well all of the pharmacological agents will be cleared so as to eliminate possible toxic interactions between the chemotherapy and the onboard drugs [47–49]. In summary, the clear increase in the global number of elderly, coupled with the concomitant later-life changes giving rise to increasing cancer rates and the potential age-related changes in the treatment of these cancers makes it essential that we develop models that can assist in our understanding of how normal aging cells and cancer cells interact.
Brief Overview of the Core Model - Model 1
A detailed discussion of the ideas behind the model can be found in . We briefly summarize that discussion in the following section.
A variety of papers, in the experimental literature, can be found to document the difference in the growth and/or proliferation rates of normal versus malignant cell lines. In particular, it is known that malignant cells can affect the growth/proliferation of surrounding normal cells. Further, the literature exhibits experimental data pointing to the fact that conjoint cultures of normal and neoplastic cells can be demonstrated to offer evidence for both the inhibition and stimulation of normal cells by these same conjoint neoplastic cells. Evidence for stimulation may be found in [50–54]. Evidence for inhibitory effects may be found in  and intermediate results are demonstrated by . Rounds(1970)  demonstrates the existence of a growth modification factor which stimulates fibroblastic growth at low concentrations, but stops mitosis and is cytotoxic at high concentrations. We summarize these results as follows. There is a growth modification factor(GMF) released by a number of malignant human cell lines. This GMF has the following properties:
At very low concentrations it does not affect fibroblast-like cells,
At intermediate concentrations it can stimulate mitotic activity,
At higher concentrations it can inhibit mitotic activity and finally,
At very high concentrations it can kill surrounding fibroblast-like cells.
A possible relationship between cancer development, metastasis, and the surrounding normal cells may be hypothesized in the following manner. Suppose that there exists a tumor cell which is releasing GMF into the surrounding population of conjointly growing normal cells. Suppose further that, due to some factor (epigenetic, environmental, immune deficiency, or aging factors), the tumor cell divides (is not inhibited by the normal inhibitory processes of the surrounding normal cells), and therefore, it produces another cell which will subsequently increase the GMF density.
It is well known that normal cells can, if the conditions are correct, control the dynamics of tumor cells. That is to say, it is possible for a collection of normal cells which surround a single tumor cell, or small number of tumor cells, to control that cell or cells and to keep their growth restrained. It is hypothesized that this might occur through interference with the mitotic phase of the tumor cells. Such effects might occur through secretion of Pardee-like labile proteins [6, 9, 58, 59]. Suppose, however, that the surrounding normal cells are unable to control the tumor cell population. Such an instance might occur, in aging tissue, when immune function has decreased and the tumor masking proteins are subsequently more effective. The inability of the normal cells to detect the tumor cells will cause a subsequent increase in the GMF titer around the developing tumor cell mass. As the titer of the GMF increases, the surrounding normal cells are killed due to the cytotoxic nature of high GMF concentrations. This toxic action makes room for subsequent divisions of the tumor cell population. In a region surrounding the tumor cell mass, but far enough away that the GMF titer is not at the toxic level, the fibroblasts are stimulated to form a surrounding boundary layer.
Several research groups have studied the growth and control of tumors from different perspectives via mathematical and theoretical modeling [60–67]. In the study of various therapeutic strategies such as chemotherapy, the major goal is to maximize the success of treatment. Therefore, in order to approach this goal, it is of critical importance to know the behavior and operation of the system that is under the influence of a given drug.
Equations (1d)-(1e) provide a generalized growth-interaction model that may serve to explain the effects of GMF on the behavior of this conjoint aging-tumor cell population mixture. The role of the GMF factor is also crucial when the coupled system of normal and tumor cells goes under a chemotherapeutic treatment. The principle aim of this study is to quantitatively expand Witten's model during the course of chemotherapy. How then do we choose the two rules f N (T) and f T (N)?
where β has the units of 1/time and ρ0 has units of cells. We will investigate this model as a first step in our discussion.
However, for our initial discussion, we will consider the simple logistic growth equation in which which reduces to our equation (2b). In the next section we discuss how this model may be modified to address chemotherapeutic intervention.
Chemotherapeutic Modification and Simulation of the Core Model
Witten's model can be extended to address the medical scenario in which a conjoint cellular system interacts with a chemotherapeutic drug: i.e., an elderly person undergoing chemotherapy. We assume that the drug kills both tumor cells and normal cells. The cellular response function to the pharmaceutical intervention can be mathematically structured as follows: F (u) = a i (1 - e-mu) where m is linked to the drug pharmacokinetics and is considered to be 1 in this preliminary study and i = N, T. In this expression, 1 - e-urepresents the chemotherapy fractional cell kill and u is the amount of the drug at the tumor site at a specific time. The coefficient of a T and a N is the response coefficient factor of the tumor cells [71–73].
The last term shows the reduction in size of each cellular population as a function of the drug interaction in that population component. In subsequent sections we discuss the simulation of the evolution of both the normal and tumor cells for various interactions.
0.1 Untreated System Evolution
We first simulated the case when the system does not interact with the drugs (the drug terms in both equations are set zero). Figure  illustrates an example of how, for the chosen set of parameters, the conjoint effect of tumor cells and normal cells on each other can be seen. As the size of the tumor cells exceeds the critical size T*, which is here considered to be T* = 3.105, the size of the normal cells N starts decreasing and the normal cells enter what we will call a inhibition phase in their population dynamics. The mini-window in the figure magnifies the behavior of the normal and tumor cells when the size of the tumor cells approaches the critical size of the tumor. In this figure the horizontal dashed line represents the critical size of the tumor cells. The system is arbitrarily considered to interact with the drug beginning at time t = 40.
Evolution of a Treated System by Static Drugs
We now address the evolution of the normal and tumor cells when the drug is static (concentration of the drug is constant) and doesn't show a concentration diffusion over time. For this purpose, u and therefore a i (1 - exp(-mu)) are considered to be constants.
In the first row of the Figure , the evolution of normal cells and tumor cells are simulated when the system interacts with a drug. It is assumed that the drug kills only tumor cells and has no effect on normal cells. As the effect of the drug increases, tumor cells show a slower growth in evolution. Therefore, their population size exceeds the critical tumor size later in time. Not only is this slower growth significant by itself, but the existence of the larger population of normal cells during the course of therapy is also distinguished. Furthermore, it is important that normal cells enter the phase of inhibition later as compared to the untreated normal cells in the untreated system.
The second row in Figure  examines the case where the drug kills both normal and tumor cells with more weight on killing the tumor cells. We have considered that the drug kills tumor cells with a specific strength. Considering this assumption, we study the system where the normal cells are killed with different strength. As the drug kills more normal cells, the seize of these cells decreases during the course of therapy, however, the normal cells enter the phase of inhibition with a delay because of the slower growth of the tumor cells caused by the drug's killing effect on tumor cells.
To summarize this section, we can see that in the untreated case, tumor cells growth fast and normal cells experience a sharp decay in their size. In the treated case, the size of the normal cells is initially maintained and the dropping behavior is delayed when just tumor cells are killed by the drug. When the drug kills both normal and tumor cells, but more tumor cells than normal cells, the decrease in the initial size of the normal cells can be detected together with a delay in entering the decaying phase.
Evolution of a Treated System by Dynamic Drugs
Model 2 - Gompertzian Tumor Growth
where h0 and γ are parameters of tumor growth. Demicheli et al. provide growth relationships and derive the two parameters for the LoVo tumor cell line.
Considering the inter-connection coupling also seen, in Figure  (top right) the normal cells enter the inhibition phase very fast and start decreasing in a very short amount of time. This behavior is associated with the fact that tumor cells grow at a very fast rate and, thus, exceed critical size in a short amount of time.
The evolution of a system treated by static drugs is also simulated in Figure . In the simulation, it is considered that the drug ideally kills just the tumor cells and has no effect on the normal cells, a N = 0. The strength of the drug is considered to begin at a T (1 - e mu ) = 0.1 and increase to a T (1 - e mu ) = 1. Returning to Figure  (top left), the size of the normal cells at the beginning of chemotherapy is almost 1.1*106. In the absence of any treatments, this size drops below 8*105. However, by interacting with an anti-tumor drug with the strength of 0.1, the normal cells experiences no drop in size.
In Model 2, the therapy begins once the normal cells enter the inhibition phase, exactly like Model 1. In this case as can be seen in Figure 4 (below, left), the size of the normal cells is almost 3.6*105 at the beginning of the therapy. With no treatments, they soon decay to zero. Implementing the drug with a strength of a T (1 - e mu ) = 0.1 maintains the size of the normal cells at 2.2*105 by the end of the therapy.
A drug with the strength of a T (1 - e mu ) = 0.17 suppresses the dropping behavior of normal cells. Based on the results of the simulation, it is evident that in order to block the decreasing behavior of normal cells a stronger drug with more power to kill tumor cells is needed in the Gompertizan tumor growth, seen in Model 2, than in the logistic tumor growth, as shown in Model 1. The behavior of the tumor cells during the therapy is also simulated above. The decrease in the size of tumor cells for two different strengths of 0.1 and 0.17 can be seen in figure 4 as well.
This work was based on a modification of Witten's conjoint tumor cell-aging fibroblast cell model . The conjoint evolution of both a normal and a tumor cell population were studied both with and without the effects of an interacting hypothetical chemotherapeutic drug.
In the absence of any drugs, the growth dynamics of the individual populations of normal and tumor cells is not independent due to the biochemical cross-talk and biomechanical interactions. In fact, the relative growth and size of the tumor/normal cell populations can control the opposing population. We note that as the size of the tumor cells exceeds a hypothetical critical size T*, the normal cells can no longer control the tumor cell population size and the population of normal cells eventually goes extinct.
The evolution of conjoint normal and tumor cell populations were then studied under the influence of chemotherapeutic drugs, and also by pre-setting model parameters such as β, ρ, and k. The system can be shown to illustrate a variety of different behaviors under a different choices of the model parameters. As the drug kills more tumor cells than normal cells, the tumor cells approach the critical size more slowly. This generates a delay in the decline of the normal cell population. Such a mechanism might allow for mixed therapeutic intervention such as joint radiation and chemotherapy. Further analysis needs to address how the model parameters might change over the chronological age of the patient and how this would affect the results of the chemotherapeutic intervention.
We conclude that the behavior of the system is complex and that the specifications of a chosen drug in terms of the decay and initial value, combined with the specifications of the system in terms of the inter-dependence of compartments during their evolution, are all critical factors shaping the behavior of the system during therapy. This knowledge may introduce a path to advance the treatment of age-related tumor development and treatment.
Future work may include the effect of the drug determining the effect of time delay in absorption at the tumor cite, or considering a kind of multiple therapy, which would combat cancer by focusing on the importance of immunotherapy and the strengthening the immune system.
All calculations were executed on an PC using Mathematica v6.0. Code is available from the first author.
- Smith JR, Whitney RG: Intraclonal variation in proliferative potential of human diploid fibroblasts: Stochastic mechanism for cellular aging. Science. 1980, 207: 82-84. 10.1126/science.7350644.View ArticlePubMedGoogle Scholar
- Witten TM: A mathematical model of genetic recombination and its relationship to aging and cancer. PhD thesis. 1974, State University of New York, BuffaloGoogle Scholar
- Witten TM: Some mathematics of recombination: Evolution of complexity and genotypic modification in somatic cells-a possible model for aging and cancer effects. Mech Aging and Dev. 1980, 13: 187-199.View ArticleGoogle Scholar
- Witten TM: Investigating the aging mammalian system: Cellular levels and beyond. Proc 25th Annual Meeting of the Society for General Systems Research, Society for General Systems Research. 1981, 309-315.Google Scholar
- Witten TM: Modeling cellular systems and aging processes: I. Mathematics of cell system models-A review. Mech. Aging and Dev. 1981, 17: 53-94. 10.1016/0047-6374(81)90128-7.View ArticleGoogle Scholar
- Witten TM: Modeling cellular aging and tumorigenic transformation. Math and Computers in Simulation. 1982, 24: 572-584. 10.1016/0378-4754(82)90661-9.View ArticleGoogle Scholar
- Witten TM: Modeling cellular systems and aging processes: II. Some thoughts on describing an asynchronously dividing cellular system. Nonlinear Phenomena In Mathematical Sciences. Edited by: Lakshmikantham V. 1982, New York City, New York: Academic PressGoogle Scholar
- Witten TM: In vitro clonal mutagenesis: A mathematical model. Advances In Computer Methods For Partial Differential Equations. Edited by: Vichnevetsky R, Stepleman RS. 1984, New Jersey: IMACS/Rutgers UniversityGoogle Scholar
- Witten TM: Population models of cellular aging: Theoretical and numerical issues. Advances in Computer Methods for Partial Differential Equations VI. Edited by: Vichnevetsky R, Stepleman RS. 1987, New Jersey: IMACS/Rutgers UniversityGoogle Scholar
- Witten TM: Modeling cellular aging: Variable cell cycle lengths. Computers in Biomedicine. Edited by: Held KD, Brebbia CA, Ciskowski RD. 1991, Southampton, England: Computational Mechanics PublicationsGoogle Scholar
- Witten TM: Some open questions in the mathematical modeling of cellular aging. Mathematical Population Dynamics: Proceedings of the Second International Conference. Edited by: Arino O, Axelrod D, Kimmel M. 1991, Marcel Dekker, NY, 16-27.Google Scholar
- Witten TM: A mathematical model for the effects of a lymphokine-like ring shaped particle on the dynamics of a conjoint tumor-normal cell culture: Some implications for the aging cancer question. Mathematics And Computers In Biomedical Applications. Edited by: DiLisi JC. 1985, New York: Elsevier/North-HollandGoogle Scholar
- Witten TM: Modeling the dynamics of conjoint tumor-normal cell culture systems: II. Further thoughts on the aging-cancer question. Modeling Of Biomedical Systems. Edited by: Eisenfeld J, Witten TM. 1986, North-Holland, AmsterdamGoogle Scholar
- Witten TM: Modeling of the aging-cancer interface: some thoughts on a complex biological dynamics. Journal of Gerontology: Biological Science, Special Issue. 1989, 44 (6): 72-80.View ArticleGoogle Scholar
- Cahill S, South K, Spade J: Outing Age: Public policy issues affecting gay, lesbian, bisexual, transgender elders. National Gay and Lesbian Task Force Policy Institute, Washington, D.C., 200
- Hooyman NR, Kiyak HA: Social Gerontology: A Multidisciplinary Perspective. 2007, New York: Allyn & BaconGoogle Scholar
- for Disease Control C: Public health and aging: Trends in aging-United States and Worldwide. AMA. 2003, 289: 1371-10.1001/jama.289.11.1371.View ArticleGoogle Scholar
- Cox RL: Global health disparities: crisis in the diaspora. J National Med Assoc. 2004, 96 (4): 546-549.Google Scholar
- Dennis EE: Aging on the world stage: Perspectives for the media on longevity with world experts on population aging. 2002, International Longevity Center-USA, New York, N.Y.Google Scholar
- Johnson NE: Aging and eldercare in lesser developed countries. J Family Issues. 2000, 21: 683-691. 10.1177/019251300021006001.View ArticleGoogle Scholar
- Kinsella K, Phillips DR: Global aging: The challenge of success. Population Bull. 2005, 60: 1-44.Google Scholar
- Kinsella K, Velkoff VA: An aging world: 2001. International population reports. 2001, U.S. Government Printing Office, Washington, D.C.Google Scholar
- on Aging: NIH NI: Why population aging matters: A global perspective. 2007, NIA/NIH Publication No. 07-6134., Washington, D.C.Google Scholar
- Aging in the Americas. Perspectives in Health Magazine of the Pan American Health Organization.http://www.paho.org/English/DD/PIN/Number19\_article02.htmhttp://www.paho.org/English/DD/PIN/Number19\_article02.htm
- Organization PAH: Health in the Americas. 1998, Pan American Health Organization, Washington, D.C.Google Scholar
- Ruger JP, Kim HJ: Global health inequalities: an international comparison. J Epidemiol Community Health. 2006, 60: 928-936. 10.1136/jech.2005.041954.PubMed CentralView ArticlePubMedGoogle Scholar
- Sykes JT: Global aging aspirations confront cultural and regional realities. The Gerontologist. 2006, 555-558.Google Scholar
- Organization WWH: Health systems: Improving performance. 2000, World Health Organization, Geneva, SwitzerlandGoogle Scholar
- World Health Organization: Aging and life course.http://www.who.int/ageing/projects/en/\quad[lastvisited8August2007]http://www.who.int/ageing/projects/en/\quad[lastvisited8August2007]
- Hawkins BA: Aging well: Toward a way of life for all people. Preventing Chronic Disease Public Health Research, Practice and Policy. 2005, 2 (3): 103-Google Scholar
- Ritchie CS, Wieland GD: Editorial: Improving end-of-life care for older adults: An international challenge. J Gerontol Med Sci. 2007, 62A (4): 393-394.View ArticleGoogle Scholar
- Burnett M: Intrinsic Mutagenesis: A Genetic Approach to Aging. 1974, New York, N.Y.: John Wiley & SonsView ArticleGoogle Scholar
- Pitot HC: Carcinogenesis and aging-two related phenomena?. A review Amer J Pathol. 1977, 87 (2): 444-472.Google Scholar
- Cohen P, Conneta B, Dix D, Flannery J: The incidence of hematologic tumours: A cellular model for, the age dependence. J theor Biol. 1981, 90: 427-436. 10.1016/0022-5193(81)90322-2.View ArticlePubMedGoogle Scholar
- Schwartz AG: Age-Related Factors which may Predispose to Carcinogenesis. 1982, USDHHS Oncology Overview, Washington, DCGoogle Scholar
- Weindruch R, Walford R: Dietary restriction in mice beginning at 1 year of age: Effect on life-span and spontaneous cancer incidence. Science. 1982, 215: 1415-1418. 10.1126/science.7063854.View ArticlePubMedGoogle Scholar
- DeVita VT: Research Frontiers in Aging and Cancer. 1982, USDHHS, NCI Monographs, Washington, DCGoogle Scholar
- Ebbesen P: Cancer and normal aging. Mech Aging and Dev. 1984, 25: 269-283. 10.1016/0047-6374(84)90001-0.View ArticleGoogle Scholar
- Macieira-Coelho A, Azzarone B: Aging, Cancer and the Lifespan of Cells in Vitro. Drugs and Aging. 1986, Berlin, Germany: Springer-VerlagGoogle Scholar
- Mathe G, Reizenstein P: Aging and human cancer. Pathophysiological Aspects of Cancer Epidemiology. Edited by: Mathe G, Reizenstein P. 1985, Oxford, England: Pergamon PressGoogle Scholar
- DePinho RA: The age of cancer. Nature. 2000, 408: 248-254. 10.1038/35041694.View ArticlePubMedGoogle Scholar
- Yanic R, Ries LAG: Cancer in older persons: an international issue in an aging world. Seminars in Oncology. 2004, 31 (2): 128-136. 10.1053/j.seminoncol.2003.12.024.View ArticleGoogle Scholar
- Bernard M, Avenin D, Selle F, Gligorov J, Houssel P, Carette B, Bourayou N, Lokiec F, Carola E, Lotz JP: Chemotherapy-induced cardiotoxicity in the elderly. Bull Cancer. 2008, 95: F89-F95.PubMedGoogle Scholar
- Hood LE: Chemotherapy in the elderly: supportive measures for chemotherapy-induced myelotoxicity. Clin J Oncol Nurs. 2003, 7 (2): 185-190. 10.1188/03.CJON.185-190.View ArticlePubMedGoogle Scholar
- Shay JW, Roninson IB: Hallmarks of senescence in carcinogenesis and cancer therapy. Oncogene. 2004, 23: 219-2933. 10.1038/sj.onc.1207518.View ArticleGoogle Scholar
- Balducci L: Aging, frailty and chemotherapy. Cancer Control. 2007, 14: 7-12.PubMedGoogle Scholar
- Balducci L: Pharmacology of chemotherapy in the older cancer patient. Cancer Control. 1999, 6 (5): 466-470.PubMedGoogle Scholar
- Lichtman SM, Villani G: Chemotherapy in the elderly: pharmacologic considerations. ancer Control. 2000, 7 (6): 548-556.Google Scholar
- Green JM, Hacker ED: Chemotherapy in the geriatric population. Clin J Oncol Nurs. 2004, 8 (6): 591-597. 10.1188/04.CJON.591-597.View ArticlePubMedGoogle Scholar
- Ludford RJ, Barlow H: Sarcomatous transformation of the stroma of mammary carcinomas that stimulated fibroblastic growth in vitro. Cancer Research. 1943, 5: 257-264.Google Scholar
- Ludford RJ, Barlow H: The influence of malignant cells upon the growth of fibroblasts in vitro. Cancer Research. 1994, 8: 694-703.Google Scholar
- Kasuta H, Takaota T, Nagai Y: Interaction in culture between normal and tumor cells of rats. Cancer Cells In Culture. Edited by: Kasuta H. 1968, Tokyo, Japan: University of Tokyo PressGoogle Scholar
- Ranadive KJ, Bhide SV: Tissue interactions in normal and malignant cells. 1962, Boston, MA: Little, Brown & CompanyGoogle Scholar
- Foley JF, Kennedy BJ, Ross JD: A factor from HeLa cells promoting colonial growth of human fibroblast-like cells in culture. Cancer Research. 1963, 23: 368-371.PubMedGoogle Scholar
- Smith AG, Cress HR: Effect of tumor deoxyribonucleic acid upon tissue cultures of fibroblasts. Lab Invest. 1951, 10: 898-907.Google Scholar
- Hymes WF, Gilbert JB, Mengoli HF, Watne AL: Inhibition of migration of rat peritoneal exudate cells by Ascites tumor fluid fractions. Nature. 1967, 213: 108-110. 10.1038/213108a0.View ArticleGoogle Scholar
- Rounds DE: A growth modifying factor from cell lines of human malignant origin. Cancer Res. 1970, 30: 2847-2851.PubMedGoogle Scholar
- Pardee AB: A restriction point for control of normal animal cell proliferation. Proc Nat Acad Sci. 1974, 7: 1286-1290. 10.1073/pnas.71.4.1286.View ArticleGoogle Scholar
- Campisi J, Medrano EE, Morreo G, Pardee AB: estriction point control of cell growth by a labile protein:Evidence for increased stability in transformed cells. Proc Nat Acad Sci. 1982, 79: 436-440. 10.1073/pnas.79.2.436.PubMed CentralView ArticlePubMedGoogle Scholar
- Laird AK: Dynamics of tumor growth. Br J Cancer. 1964, 18: 490-498.PubMed CentralView ArticleGoogle Scholar
- Bajzer B, Carr T, Josic K, Russell SJ, Dingli D: Modeling of cancer virotherapy with recombinant measles viruses. Journal of theoretical Biology. 2008, 252: 109-122. 10.1016/j.jtbi.2008.01.016.View ArticlePubMedGoogle Scholar
- Dingli D, Cascino MD, Josic K, Russell SJ, Bajzer Z: Mathematical modeling of cancer radiovirotherapy. Mathematical Biosciences. 2006, 199: 80-103. 10.1016/j.mbs.2005.11.001.View ArticleGoogle Scholar
- Kozusko F, Bajzer Z: Combining Gompertzian growth and cell population dynamics. Mathematical Biosciences. 2003, 185: 153-167. 10.1016/S0025-5564(03)00094-4.View ArticlePubMedGoogle Scholar
- Kozusko F, Bourdeau M, Bajzer Z, Dingli D: A microenvironment based model of antimitotic therapy of Gompertzian tumor growth. Bull Math Biol. 2007, 69 (5): 1691-10.1007/s11538-006-9186-5.View ArticlePubMedGoogle Scholar
- Wodarz D: Viruses as antitumor weapons: defining conditions for tumor remission. Cancer Res. 2001, 61: 3501-3507.PubMedGoogle Scholar
- Wodarz D: Gene therapy for killing p53-nagative cancer cell: use of replicating versus non replicating agents. Hum Gene ther. 2003, 14: 153-159. 10.1089/104303403321070847.View ArticlePubMedGoogle Scholar
- Feizabadi MS, Volk C, Hirschbeck S: A two-compartment model interacting with dynamic drugs. Applied Mathematics Letters. 2009, 22: 1205-1209. 10.1016/j.aml.2008.12.003.View ArticleGoogle Scholar
- Narayan KS, Rounds DE: Minute ring shaped particles in cultured cells of malignant origin. Nature New Biol. 1973, 243: 146-150. 10.1038/243146a0.View ArticlePubMedGoogle Scholar
- Rounds DE, Narayan KS, Levan NE: Production of ring shaped particles by normal and metastatic tissue. 1. Human Skin. J National Cancer Institute. 1975, 55: 7-10.Google Scholar
- Sachs RK, Hlatky LR, Hahnfeldt P: Simple ODE models of tumor growth and anti-angiogenic or radiation treatment. ath and Computer Modeling. 2001, 33: 1297-1305. 10.1016/S0895-7177(00)00316-2.View ArticleGoogle Scholar
- de Pillis LG, Radunskaya A: The dynamics of an optimally controlled tumor model:A case study. Mathematical and Computer Modeling. 2003, 37: 1221-1244. 10.1016/S0895-7177(03)00133-X.View ArticleGoogle Scholar
- de Pillis LG, Gu W, Radunskaya A: Mixed immunotherapy and chemotherapy of tumors: modeling, applications and biological interpretations. J theor Biol. 2006, 238: 841-862. 10.1016/j.jtbi.2005.06.037.View ArticlePubMedGoogle Scholar
- Panetta JC: A mathematical model of breast and ovarian cancer treated with Paclitaxel. Mathematical Biosciences. 1997, 146: 89-113. 10.1016/S0025-5564(97)00077-1.View ArticlePubMedGoogle Scholar
- Bassukas ID: Comparative Gompertzian analysis of alterations of tumor growth patterns. Cancer Res. 1994, 54: 4385-4392.PubMedGoogle Scholar
- Norton L: A Gompertzian model of human breast cancer growth. Cancer Res. 1988, 48: 7067-7071.PubMedGoogle Scholar
- Demicheli R, Foroni R, Ingrosso A, Pratesi G, Soranzo C, Tortoreto M: An exponential-Gompertzian description of LoVo cell tumor growth from in vivo and in vitro data. Cancer Res. 1989, 49: 6543-6546.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.