Combined changes in Wnt signaling response and contact inhibition induce altered proliferation in radiation-treated intestinal crypts.

Curative intervention is possible if colorectal cancer is identified early, underscoring the need to detect the earliest stages of malignant transformation. A candidate biomarker is the expanded proliferative zone observed in crypts before adenoma formation, also found in irradiated crypts. However, the underlying driving mechanism for this is not known. Wnt signaling is a key regulator of proliferation, and elevated Wnt signaling is implicated in cancer. Nonetheless, how cells differentiate Wnt signals of varying strengths is not understood. We use computational modeling to compare alternative hypotheses about how Wnt signaling and contact inhibition affect proliferation. Direct comparison of simulations with published experimental data revealed that the model that best reproduces proliferation patterns in normal crypts stipulates that proliferative fate and cell cycle duration are set by the Wnt stimulus experienced at birth. The model also showed that the broadened proliferation zone induced by tumorigenic radiation can be attributed to cells responding to lower Wnt concentrations and dividing at smaller volumes. Application of the model to data from irradiated crypts after an extended recovery period permitted deductions about the extent of the initial insult. Application of computational modeling to experimental data revealed how mechanisms that control cell dynamics are altered at the earliest stages of carcinogenesis.

Exogenous expression of beta-catenin regulates contact inhibition, anchorage-independent growth, anoikis, and radiation-induced cell cycle arrest.

beta-Catenin is an important regulator of cell-cell adhesion and embryonic development that associates with and regulates the function of the LEF/TCF family of transcription factors. Mutations of beta-catenin and the tumor suppressor gene, adenomatous polyposis coli, occur in human cancers, but it is not known if, and by what mechanism, increased beta-catenin causes cellular transformation. This study demonstrates that modest overexpression of beta-catenin in a normal epithelial cell results in cellular transformation. These cells form colonies in soft agar, survive in suspension, and continue to proliferate at high cell density and following gamma-irradiation. Endogenous cytoplasmic beta-catenin levels and signaling activity were also found to oscillate during the cell cycle. Taken together, these data demonstrate that beta-catenin functions as an oncogene by promoting the G(1) to S phase transition and protecting cells from suspension-induced apoptosis (anoikis).

A generalized state-vector model for radiation-induced cellular transformation.

A mathematical model is developed, detailing the manner in which radiation brings about the transformation of cells to a state of uncontrolled growth. The model is based on the concepts of initiation and promotion, with the irradiation acting both to damage intracellular structures and to change the state of cells surrounding a damaged (initiated) cell. The complete model requires that the radiation produce two forms of damage within a cell, with at least one of the forms requiring an interaction which is a function of time since irradiation. Some form of contact inhibition must be removed, with this step being a function of the probability that a cell in an initiated state will be surrounded by n dead cells. The cell then must divide, with the probability of moving the cell to the final transformed state being a function of the number of cellular divisions. Prior to irradiation, it is assumed that cells may be characterized by an initial state vector describing the probability that any given cell is in one of the states specified by the model. The resulting model then is used to explain data concerning in vitro irradiation of cells by acute doses of X-rays, alpha particles and neutrons. Limited tests of the theory under conditions of fractionated irradiation are also provided. A controlling factor in such studies is the number of cells already in intermediate states prior to the irradiation.

Long-term effects of gamma-irradiation on cultured human thyroid cells.

When differentiated 15-day-old cultures of human thyroid glands were irradiated they exhibited a high degree of radiosensitivity, an absence of split-dose recovery, an increase in the number of non-senescent colonies observed over four passages, increased focus formation on the confluent postirradiation monolayer and a shift in the isozyme pattern of LDH towards the anaerobic form (LD 5). The effects are similar to those previously observed for irradiated sheep thyroid cultures, but occurred at lower radiation doses.

Absence of contact effects in irradiated EMT6-Rw tumors.

Some cells have been reported to show greater resistance to drugs or radiation when growing with close intercellular contacts in spheroids or in solid tumors than when growing with few intercellular contacts in sparse cultures. In some cases this increased resistance reflects an increased capacity of cells in close contact to repair cytotoxic damage. However, not all tumors show contact effects, and in some tumors and spheroids the increased resistance appears to be produced by environmental factors, such as hypoxia, rather than by changes in the repair capacity of the cells. To assess whether EMT6-Rw cells showed increased intrinsic radioresistance when grown as solid tumors, we compared survival curves for cells in exponentially growing monolayers and in solid tumors in BALB/c mice. To avoid complications arising from regional heterogeneity in oxygenation within solid tumors, these irradiations were performed under conditions of uniform, maximal hypoxia. The two survival curves were indistinguishable. Moreover, survival curves for cells suspended from solid tumors, plated at low densities and irradiated immediately, after 5 h of incubation or after 24 h of incubation, were indistinguishable from one another and were indistinguishable from survival curves for cells suspended from exponentially growing monolayers and irradiated immediately using an identical protocol. It therefore appears that contact effects are insignificant for irradiated EMT6-Rw tumors and that the intrinsic radiosensitivity of these cells is similar in culture and in solid tumors.