Tumor response to radiotherapy is dependent on genotype-associated mechanisms in vitro and in vivo
© Williams et al. 2010
Received: 9 June 2010
Accepted: 12 August 2010
Published: 12 August 2010
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© Williams et al. 2010
Received: 9 June 2010
Accepted: 12 August 2010
Published: 12 August 2010
We have previously shown that in vitro radiosensitivity of human tumor cells segregate non-randomly into a limited number of groups. Each group associates with a specific genotype. However we have also shown that abrogation of a single gene (p21) in a human tumor cell unexpectedly sensitized xenograft tumors comprised of these cells to radiotherapy while not affecting in vitro cellular radiosensitivity. Therefore in vitro assays alone cannot predict tumor response to radiotherapy.
In the current work, we measure in vitro radiosensitivity and in vivo response of their xenograft tumors in a series of human tumor lines that represent the range of radiosensitivity observed in human tumor cells. We also measure response of their xenograft tumors to different radiotherapy protocols. We reduce these data into a simple analytical structure that defines the relationship between tumor response and total dose based on two coefficients that are specific to tumor cell genotype, fraction size and total dose.
We assayed in vitro survival patterns in eight tumor cell lines that vary in cellular radiosensitivity and genotype. We also measured response of their xenograft tumors to four radiotherapy protocols: 8 × 2 Gy; 2 × 5Gy, 1 × 7.5 Gy and 1 × 15 Gy. We analyze these data to derive coefficients that describe both in vitro and in vivo responses.
Response of xenografts comprised of human tumor cells to different radiotherapy protocols can be reduced to only two coefficients that represent 1) total cells killed as measured in vitro 2) additional response in vivo not predicted by cell killing. These coefficients segregate with specific genotypes including those most frequently observed in human tumors in the clinic. Coefficients that describe in vitro and in vivo mechanisms can predict tumor response to any radiation protocol based on tumor cell genotype, fraction-size and total dose.
We establish an analytical structure that predicts tumor response to radiotherapy based on coefficients that represent in vitro and in vivo responses. Both coefficients are dependent on tumor cell genotype and fraction-size. We identify a novel previously unreported mechanism that sensitizes tumors in vivo; this sensitization varies with tumor cell genotype and fraction size.
Much research in clinically-relevant radiobiology is based on the premise that there is a triangular relationship between radiocurability of tumors in the clinic, radiosensitivity of xenograft tumors in vivo and radiosensitivity of human tumor cells in vitro. We have previously reported, in collaboration with Vogelstein's laboratory, that abrogation of a single gene (p21) increases susceptibility of xenograft tumors to radiotherapy but compared to its parent line, does not effect in vitro radiosensitivity . This was the first report showing modulation of a single gene could uncouple in vitro versus in vivo radiosensitivity. It also implies that in vitro radiosensitivity alone cannot predict tumor response.
We now compare in vitro and in vivo responses of multiple human tumor cells that vary in radiosensitivity and genotype. We selected a set of human tumor cells from a large study that defined radiosensitivity as measured in vitro. These cell lines segregated into radiosensitivity groups and each group associated with genotype, not histological type [2, 3]. When these data are placed in an appropriate structure, tumor cell radiosensitivity segregates into distinct groups that each associate with a specific genotype. Four genotypes were identified that were markers for these radiosensitivity groups: mutant ATM, wildtype TP53, mutant TP53 and an unidentified gene or factor (glio) that renders a subset of glioblastoma cells very radioresistant [2, 3]. These cell lines represent the most sensitive cell line we have examined (SW1222), the most resistant cell lines we have examined (U251) and six cell lines that represent the most common genotypes expressed in human tumor cells, wtTP53 and mutTP53. We now define in vivo radiosensitivity of xenograft tumors comprised of these cell lines that represent these four cellular radiosensitivity groups. We stress that while we selected cell lines from each radiosensitivity group, we did not select specific genotypes. Oncogenesis selected the four genotypes that segregate with tumor radiosensitivity.
Critical to interpreting our data is confidence that xenograft tumors reflect relevant properties of cellular radiosensitivity. Xenograft tumors have been demonstrated to be a useful general tool for studying in vivo radiosensitivity compared to in vitro characteristics of their constituent cells [4–6]. Xenograft studies have been particularly useful in studying the dose-rate effect , the effect of dose-fractionation [8, 9] identification of the α/β ratio  and the role of TP53 in tumor response . Xenograft studies have been used to seek correlations between in vitro and in vivo response for tumors of different histological types, including melanoma , breast , lung , colon , glioblastoma  and squamous cell carcinoma . We have previously used xenograft studies to show abrogation of a single gene, CDKN1A (p21), increases xenograft tumor radiosensitivity to large fractions (15 Gy) in vivo but does not alter cellular radiosensitivity in vitro . Similarly some genomic manipulations increase sensitivity to other anti-cancer agents but not ionizing radiation .
Multiple methods have been used to describe quantitative response of xenograft tumors to radiotherapy. For instance the use of TCD50 (mean dose required to inhibit regrowth in 50% of tumors) is a powerful yet resource-intensive method . We and others have used direct comparison of kinetics of regrowth delay between pairs of tumor types or between pairs of radiotherapy protocols [1, 18] and while this method has significant statistical power in such a pair-wise comparison, it is limited in comparing response of multiple tumors that vary widely when irradiated with different radiotherapy protocols. We now study the response of multiple cell lines that vary extensively in genotype and susceptibility to cell killing in vitro, for the relative sensitivity of their xenograft tumors in vivo. It was important to measure tumor response over a wide range of cell and tumor sensitivities so we selected a modification of the method of Schwachofer et al  to describe tumor response to radiotherapy based on modal volume of regrowing tumors even when some tumors do not regrow. These methods are described below.
Human colorectal tumor cell lines (HCT116, 80S4, 14-3-3σ-/-, 379.2, DLD1 and 19S186) were obtained from Dr. B. Vogelstein of the Oncology Center of Johns Hopkins, School of Medicine), SW1222 was from Dr. James Russell (Memorial Sloan-Kettering Cancer Center, NY), and U251 was purchased from ATCC. The basic media for all colon tumor cell lines was McCoy 5A, supplemented with 10% FBS, 1% penicillin and streptomycin, 1% L-glutamine; 14-3-3σ-/- required addition of G418 (0.5 mg/ml); SW1222 was grown in RPMI 1640. Human glioma cell line U251 was cultured in DMEM/F12 with 10% FBS, 1% L-glutamine and 1% Penicillin and streptomycin. All cells were sub-cultured twice a week to maintain exponential growth.
Cells were plated ~18 hours before irradiation. Surviving colonies were determined 10-14 days after irradiation depending on the cell line. Cells were stained with crystal violet and colonies counted (>50 cells/colony). Additional plates for each experiment were used as microcolony controls.
Cells were irradiated using a 137Cs AECL Gammacell40 gamma irradiator at 0.7 Gy/min. For irradiation of xenograft tumors, mice were confined in 50 ml plastic centrifuge tube with holes through which the tail and the tumor-bearing leg could be extended. Tumors were irradiated at dose rate of 7.5 Gy/min with a collimated beam in a J.L. Shepard Mark I 137Cs irradiator (Pasadena CA USA).
Tumors were established by subcutaneous injection of 5 million cells suspended in PBS into the upper thigh of nude mice. Each cohort included 6 to 13 tumors. Tumor growth rate was determined by measuring three orthogonal diameters of each tumor twice a week and the tumor volume estimated as π/6[D1 × D2 × D3], when individual tumor volumes reached ~0.1-0.3 cm3, radiation treatment was initiated. Modal specific growth delay (mSGD) was measured for all cohorts in which a majority of tumors reached a volume four times the initial volume. Response was normalized to growth of unirradiated cells. We chose not to use the mean of specific regrowth delay patterns since a significant proportion of our cohorts included one or more tumors that did not regrow. Thus the mean became limited as a regrowth parameter. In our forty xenograft experiments, only cohorts of the very sensitive (VS) cells, SW1222, less than half the tumors regrew when treated with 7.5 and 15.0 Gy and thus the modal values for SGD are no longer meaningful. For these two cohorts we estimated mSGD based on the regrowth pattern for the minority of tumors that did regrow. When we tested the sensitivity of modal to mean growth delay in selected cohorts in which all tumors regrew, the modal value always fell within one standard deviation of the mean. These methods share some characteristics of the methods described by Schwatchofer . To provide an overview of the dichotomous response when some tumors regrow but some do not, we indicated such cohorts with an arrow showing this value, in terms of overall tumor response, was the common minimum response.
Comparison of data clusters were evaluated using Student's t test with p < 0.05 as the level for significance.
Our data are presented as three major observations: 1) In vitro radiosensitivity of tumor cells and in vivo radiosensitivity of their xenograft tumors show specific relationships that vary with genotype; 2) this large data matrix can be structured into an analytical system based on two coefficients that describe in vitro and in vivo radiosensitivity in parametric terms; and 3) these comparisons demonstrate a new heretofore unrecognized mechanism that influences in vivo radiosensitivity.
Genetic variation and in vitro radiosensitivity of eight human tumor cell lines.
In Vitro Radiosensitivity
Most resistant cell line, other radioresistant glioblastomas segregate into this group.
Other epithelial tumors that express mutTP53 segregate into this group.
p21 double knockout from DLD1
Other epithelial tumors that express wtTP53 segregate
into this group.
p53 double knockout from HCT116.
p21 double knockout from HCT116
14-3-3σ double knockout from HCT116
Most sensitive cell line, mutant in the ATM gene with an A moiety inserted in codon 6997 of exon 50.
These data represent the range of human tumor cell radiosensitivity as observed across a large cohort of human tumor cells. Each radiosensitivity group expresses a common genotype and each clonogenic inactivation in each group is statistically distinct at circa 2 Gy. However the distribution of tumor cell radiosensitivity with genotype is better seen when radiosensitivity of tumor cells is expressed as the ratio of radiosensitivity at circa 2 Gy and radiosensitivity at higher doses. In references [2, 3] we have designated the four cellular radiosensitivity groups as VS (very sensitive), S (sensitive), R (resistant) and VR (very resistant) based on statistical differences in survival at 2 Gy. The four groups of tumor cells are statistically different in survival levels at circa 2 Gy. However the overall relationship between genotype and in vitro radiosensitivity is better illustrated when shown as correlation between two slopes that represent clonal inactivation over two dose ranges.
These data are shown in figure 2 as four linear arrays, each array comprised of a radiosensitivity group that share genotype. Most human tumor cell lines established from clinical specimens fall into two radiosensitivity groups, S and R. Tumor cells that fall into the S radiosensitivity group express predominantly, but not exclusively, wtTP53. Indeed a cell line (379.2) that has been abrogated in TP53 as a mature cancer cell, shares the S response even though null for TP53 expression. The S cell group also includes sublines of the colorectal tumor line HCT116 that have been abrogated in CDKN1A, p21 (80S4 cells) or abrogated in 14-3-3 σ (14-3-3σ-/-). 80S4 cells (p21-) are from the cell line that we showed have increased radiosensitivity as xenograft tumors . The R radiosensitivity group is comprised predominantly, but not exclusively, of cells that express mutTP53. In our studies the R radiosensitivity group is represented by DLD-1 that expresses mutTP53 and one subline that has been abrogated in CDKN1A, p21 (19S186). VS cells (SW1222 cells) are mutant in ATM (an A moiety inserted in codon 6997, codon 50) and this is the most sensitive cell line we have identified. A VR cell line (U251 cells) is representative of the most radioresistant group of human tumor cells. Importantly, four cell lines in figures 1 and 2 show diminished levels of p21 expression: 80S4 cells, that represents abrogation of p21 in a wildtype TP53 background; 19S186 cells represent abrogation of p21 in a mutant TP53 background; the cell line mutant in ATM and the radioresistant glioblastoma line. The data in figures 1 and 2 show that abrogation of p21, 14-3-3σ and surprisingly TP53 does not modulate in vitro radiosensitivity. The fact that abrogation of TP53 does not shift radiosensitivity from the S group demonstrates that the presence of wtp53 protein is not involved in the expression of S radiosensitivity observed in all cells that express wildtype TP53.
These data, representing over 3000 individual data, show an extremely wide range of in vivo radiosensitivity for different genotypes on the basis of protocols. Certain general observations can be made before detailed analysis. First, response of tumors comprised of SW1222 (mutATM) cells are hypersensitive to all protocols, both fractionated and acute. Total dose dominates responses of this cell lines and sparing by fractionation is not as effective as other cell lines. Surprisingly the most resistant cell line U251 is unexpectedly sensitive to larger fractions. In general cells from the R group are more resistant over most protocols compared to the S group.
The wide range of data in this figure demonstrates how the use of modal SGD allows estimation of a single parameter over all cell types and protocols. Only for two cohorts, VS cells treated with 15 Gy acute or 16 Gy delivered as 8 fractions, did fewer than half the tumors failed to regrow shown as terminal values observed at day 34 for the 8 × 2 Gy cohort and at 40 days for the 1 × 15 Gy treatments. In figure 3, these cohorts we draw a dotted line representing the response of the tumors that did regrow but constituted less than half the total tumors in the cohort.
To indicate the effect of dichotomous response, wherein all tumors in a cohort did not regrow, we indicate these with a short arrow at the value of mSGD where measurements are made.
Four cell lines in figure 3 show exceptional levels of regrowth delay after irradiation with single fractions of 15 Gy and these are: SW1222 (mutATM), 80S4 (wtp53, p21-), 19S186 (mutTP53, p21-) and U251 (radioresistant glioma "glio"). Based on our previous work  we expected this elevated response for tumors comprised of cells abrogated in p21(80S4 cells, p53+, p21-) and perhaps for SW1222 (mutATM) cells that have exceptional radiosensitivity in vitro, but the response of 19S186 cells (mutp53, p21-) and especially the response of U251 cells (glio) were not expected. On the basis of this clear dichotomy in response to 15Gy expressed by tumors comprised of four cell lines compared to the other four lines we will present and analyze our data on the basis of two response groups, one designated the "S-R response group" and postulate it represents most cell lines that fall into the S and R radiosensitivity groups. The other group will be identified at this point as "p21- response group" and includes two cell lines abrogated in p21 (80S4 and 19S186) and two cell lines shown in table 1 to express diminished p21 (SW1222 cells and U251 cells).
In the next several figures we propose a simple analytical structure that can be used to compare in vitro and in vivo radiosensitivity.
These data show that tumor genotype influences response of xenograft tumors to radiotherapy. These data segregate data into two different response patterns. The correlation between xenograft responses for four genotypes shown in the left hand panel is a relatively linear relationship between tumor response and log of total-cells-killed but the xenografts responses for four other genotypes as shown in the right hand panel, are distinctly elevated. For both panels, the arrows pointing to the right indicate that modal Specific Growth Delay was determined by the majority of tumors in the cohort but that one or more tumors did not regrow. Thus the data points with arrows are an estimate of minimum regrowth delay.
The data in the left hand panel show relatively strong correlation between tumor response and logs of total-cells-killed with a relatively high correlation coefficient of 0.7271, a surprisingly strong correlation for data derived from multi-factor biological experiments. We will refer to this group for the benefit of discussion as the S-R tumor radiosensitivity group as the tumors in this panel are comprised of four cell lines from the S and R cellular radiosensitivity groups. The four genotypes that fall into the more linearly responding tumors are comprised of cells that include 3 lines that are in the S radiosensitivity group: HCT-1116 (wtTP53) and two sublines abrogated in TP53 (379.2) and 14-3-3σ (14-3-3σ -/-). It also includes one cell line from the R radiosensitivity group DLD-1 (mutTP53). Even though S cells in general are more sensitive than R cells in vitro, representatives of both groups fall into the same, relatively linearly responding tumor radiosensitivity group. We will examine this relationship in more detail below.
The patterns of tumor radiosensitivity in the right hand panel of figure 4 are significantly different, showing a more sensitive response, especially at higher doses and larger fraction sizes. While we previously documented this increased response in 80S4 cells (wtTP53 p21-/-), increased sensitivity of other three cell lines; 19S186 cells (mutTP53 p21-/-); SW1222 cells (mutATM) and U251 cells (glio) was unexpected, especially U251 which is a very resistant glioblastoma cell line based on in vitro radiosensitivity. We interpret the data in the right hand panel of figure 4 to demonstrate a heretofore undocumented mechanism that renders some tumors significantly more sensitive to radiotherapy. For the purpose of discussion we will designate these as the p21- tumor radiosensitivity group since all cell show diminished expression of p21 (table 1). In the p21- tumor radiosensitivity group there is a strong effect observed at higher dose-fractions, particularly 15 Gy. We emphasize that this designation does not imply necessarily that p21 is directly involved in tumor radiosensitivity although this relationship needs further investigation.
The data in figure 4 can be expressed as a relationship between observed tumor response and logs of total-cells- killed, but this relationship is clearly different between tumor cells in the left hand panel and right hand panel. Therefore the overall relationship between tumor responses described in Modal Specific Growth Delay to total dose is not a simple linear relationship but must be expressed in terms of at least two factors that influence quantitative variation across genotype, fraction size and total dose.
In equation 1, TR (tumor response) is expressed in days of modal specific growth delay (mSGD) and is a function of genotype G, total dose nd delivered in fractions size d. The two modifying coefficients τ and ρ vary with genotype and fraction-size. The factor τ represents in vitro radiosensitivity expressed as the ratio of total-cells-killed in vitro per unit dose. The factor ρ represents a coefficient that expresses additional in vivo radiosensitivity that cannot be accounted for by cell killing. We emphasize that the relationship in equation 1, is specific to genotype, fraction size and total dose as indicated by subscripts.
These patterns are a direct portrayal of the changes in cell killing for the four protocols derived from the survival curves in figure 1.
These data show significant differences in vivo radiosensitivity between the two groups of tumor genotypes. The major differences are at higher doses and for single fractions.
In this set of cells and protocols, τ varies between cell lines up to a factor of ~12 (U-251 versus SW1222) and between different protocols in a single cell line up to a difference of up to a factor ~6 (DLD-1 cells, 15 Gy acute versus 8 × 2 fractionated).
The data in figure 8 represent additional tumor response per Gy for observed tumor response for the eight genotypes and four radiation protocols. The data in figure 8 show remarkably similar values of ρ for the S-R response group over all doses but elevated levels for the p21- response (80S4 and 19S186) only for single doses of 15 Gy. Elevated levels for all responses for the VS response (SW1222 cells); and surprisingly, much elevated values for the VR response (U251 cells). When the 16 values of ρ for the S-R responses are compared to the 16 values of cells from the other response groups there is a highly significant difference (p < 0.005).
Data in this figure resolve tumor response into multiple, distinct clusters of data based on the parameters τ and ρ. Heavy arrows identify the pronounced increase response to 15 Gy for five cell lines. Four tumor response groups are identified and these correspond to the four in vitro radiosensitivity groups identified in figure 1. In figure 9 these groups are further defined on the values of the parameters τ and ρ. The S and R response groups share similar values of ρ but are statistically different based on τ. A VS response group is defined by significantly increased values for both τ and ρ. The VR group is defined by significantly lower values of τ than all other cell lines but highest values of ρ. Two data points for 379.2 cells (abrogated TP53) fall between the S and R groups. The four groups are statistically different based on t-test analyses with p < 0.05 as the criterion for significance.
These data demonstrate that tumor response varies strongly based on fraction size and tumor cell genotype.
These data demonstrate genotype-dependent variation in predicted tumor response. The extent of this variation based on genotype and fraction-size has a range of approximately 14, a remarkable difference for protocols that deliver the same total dose. The schema at the bottom of this figure identifies the relationship between in vitro cellular radiosensitivity groups and in vivo tumor radiosensitivity groups.
Our studies demonstrate three major observations.
1) We have established a major data base comparing radiosensitivity in vitro and xenograft tumor response in vivo for human tumor cells that represent the range of human tumor cell radiosensitivity. These data segregate with tumor cell genotypes that become markers for in vivo radiosensitivity response groups.
2) We have developed an analytical structure that predicts response of tumors to different protocols based on tumor cell genotype and fraction size. This structure separates the effects of genotype, fraction size and total dose on tumor radiosensitivity. This structure is based on defining two coefficients, each representing different independent mechanisms. One coefficient defines TCK (total cell killing (TCK) as measured in vitro. The second coefficient defines additional effects in vivo that are not predicted by TCK. Both coefficients vary with genotype and fraction-size.
3) We have defined a heretofore unreported mechanism of in vivo radiosensitivity that is dependent on tumor cell genotype and fraction size. This mechanism can dominate tumor response but is only observed in some genotypes and for larger fractions.
The data in figures 1, 2 and 3 define groups of tumor cells that share in vitro radiosensitivity and share expression of specific genotypes. We have used this variation in tumor cell radiosensitivity to define four radiosensitivity groups. Our analysis of tumor response as it relates to genotype now allows us to define "tumor response groups". These groups are represented by their values of τ and ρ and are listed below.
1) S (wtTP53) tumor response: This tumor response is represented in this paper by cell lines from the S radiosensitivity groups that express wtTP53. We have identified 17 cell lines that share this radiosensitivity group and each expresses wtTP53 . Cells abrogated in TP53 [2, 3] also fall into this radiosensitivity group and hence the radiosensitivity of this group does not reflect the direct contribution of the wtp53 protein. In figure 11 we use the response of one of these cell lines, HCT116 to 60 Gy delivered as 2 Gy fractions as a basis for comparison for other genotypes and other fraction sizes.
2) R (mutTP53) response. This response is represented by cell lines from the R radiosensitivity group that express predominantly but not exclusively, mutTP53. We have identified 14 cell lines that share this cellular radiosensitivity  and together with the S radiosensitivity group these two radiosensitivity groups represent over 90% of human tumor cell lines that we have examined. These cell lines share a common value of ρ with the S tumor response group indicating similar in vivo mechanisms of response but differ in values of τ directly related to their decreased radiosensitivity in vitro.
2) VS (mutATM) tumor response: This response is observed in xenograft tumors comprised of a single cell line (SW1222) which is mutated in the ATM gene. We have shown SW1222 cells to be extremely radiosensitive and show dramatically increased expression of apoptosis and dysfunctional progression in the cell cycle . The VS response is characterized by the highest values of τ (in vitro radiosensitivity) of cells but also shows an increase in response in ρ compared to S and R responses. Additionally, this response includes enhanced sensitivity to a single large fractions (15 Gy), a property shared with other cell lines that express diminished p21.
3) VR ("glio") tumor response. The VR group is represented by a single cell line in these studies, the radioresistant glioblastoma cell line U251. We predict, however, that other radioresistant cell lines that share extreme in vitro radioresistance may share this tumor response [2, 3]. Tumors comprised of U251 cells are characterized by the most resistant intrinsic cellular sensitivity in vitro (smallest τ) we have observed but are characterized, surprising to us, the highest values of ρ for any cell line, particularly for larger single fractions. If this is a characteristic of all radioresistant glioblastoma lines, it not only suggests a rationale for large-fraction therapy of brain tumors but also offers a more precise clinical strategy for attacking this class of tumors. We caution, however, that our studies were performed with tumors implanted in the flanks of nude mice. We do not know whether glioblastomas within the cranium would respond in a similar way.
4) p21- tumor response to larger fraction-size: This response is observed in five cell lines and is characterized at the cellular level by diminished expression of p21 (DLD-1, 19S186, 80S4, SW1222 and U251) and at the tumor level by common enhanced sensitivity only to large fractions (15 Gy). Note that in our overall classification, we place both DLD-1 and its subline 80S4 that is abrogated into R cellular radiosensitivity group and both exhibit increased response to 15 Gy, but the relative response of the line abrogated in p21 results into increased sensitivity of this subline similar to the exaggerated response to 15 Gy by the S cell line abrogated in p21, or the other three cell lines in the p21- response group. While only two of these lines are abrogated in the CDKN1A (p21) gene, the other three cell lines show diminished p21 induction as measured by Western blot analysis. Others have reported cells with deficient ATM  and radioresistant glioblastoma cells [23, 24] express diminished p21 in vivo. We caution that we have certainly not proved that diminished p21 expression in vivo is the mechanism that underlies increased radiosensitivity at higher doses; however it is clearly associated statistically. To us it is an attractive hypothesis but proof will require extensive, detailed assay in vivo in tumors irradiated with smaller and larger doses in which p21 expression, VEGF levels, microvessel density, apoptosis and cell necrosis are measured in p21- tumors compared to genotypes that are competent in the expression of this gene expression.
Our studies define an experimental system that can identify genes that do or do not influence tumor response. Genes that influence tumor response can be described as modifying ρ or τ or both. The ratio τ is influenced by wtTP53, mutTP53, mutATM and glio but not by abrogated p21. The ratio ρ is influenced by mutATM, abrogated p21, and glio. Abrogated TP53, abrogated CDKN1A, 14-3-3σ, hMLH2 and hMSH6 do not influence in vitro radiosensitivity as measured in our studies. 14-3-3σ, hMLH2 and hMSH6 do not influence tumor radiosensitivity in vivo.
We have previously hypothesized that differences in τ may reflect an influence of chromatin structure on radiosensitivity including access to repair and modulation of apoptosis [1, 2] This is supported by several reports: the protective influence of p53 on chromatin structure  and chromatin structure as a target for radiation-killing ; influence of chromatin structure on repair . We have also previously shown that depletion of polyamines in chromatin sensitizes cells to ionizing radiation delivered at higher doses, Williams et al . Importantly, Hittelman and Pandita  have shown radiosensitivity associated with ATM results from an essential difference in chromatin structure that modulates processing of radiation damage. These several reports support the hypothesis that variation in radiosensitivity between the cellular radiosensitivity groups is attributable to changes in chromatin structure that develop during oncogenesis.
In vivo radiosensitivity, we hypothesize, reflects changes in ρ observed in the several tumor response groups and may reflect interactions between tumor cell genotype and the tumor microenvironment. We do not know what mechanism underlies the relationship between diminished p21 (p21- response); enhanced cellular apoptosis (VS response); and an enhanced, but unidentified, effect observed in radioresistant glioblastoma cells (VR response). However the differences between in vivo radiosensitivity and p21 expression can be studied using the model systems we have developed. Interestingly, Kuljaca et al  have shown that p21 promotes angiogenesis so the interaction of p21 with angiogenesis at higher doses needs further study. Importantly, the creation of an appropriate tumor microenvironment that would enhance tumor response may be achievable using chemical or biological agents.
We make the following overall hypothesis for the relationships between tumor cell genotype, intrinsic cellular radiosensitivity and tumor radiosensitivity:
Tumor cell genotype, used in the broadest sense to include chromatin conformation, correlates with: 1) intrinsic cellular radiosensitivity as defined by clonogenic survival in vitro; and 2) enhanced tumor response in vivo for some genotypes at higher doses reflecting an interaction between tumor cell genotype and the tumor microenvironment. These two mechanisms act independently but together can predict tumor response to different radiotherapy protocols based on tumor cell genotype, fraction size and total dose.
cells that express most common form of in vivo radiosensitivity. P21- cells exhibit increased in vivo radiosensitivity and all are deficient or reduced in expression of p21.
modal specific growth delay.
We acknowledge the contribution of Dr. Bert Vogelstein and Ken Kinsler for providing human colorectal tumor cell lines. Dr. James Russell provided the SW1222 cells and Dr. Larry Dillehay collaborated in performing the in vivo studies.
Supported by PO-CA79862 to JRW and the Department of Radiation Medicine of Loma Linda Medical Center.
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