Delayed heritable damage and epigenetics in radiation-induced neoplastic transformation of human hybrid cells

Marc Mendonca, R. J. Antoniono, J. L. Redpath

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

The HeLa x skin fibroblast human hybrid cell system has proven to be an excellent model system for quantitative studies of radiation-induced neoplastic transformation in vitro. A unique aspect of this system is the reexpression of a cell surface protein p75/150 with tumorigenicity. The identification of p75/150 as intestinal alkaline phosphatase (IAP) allowed for the recent development of a more simplified, rapid, and sensitive screening method than the previous p75/150 antibody-based staining procedure. The new method directly detects neoplastically transformed, IAP-expressing cells by staining with the alkaline phosphatase chromogenic substrate, Western Blue (WB). Earlier studies with the antibody-based immunoperoxidase assay indicated that, while no foci with tumor-associated antigen (p75- positive) were evident 15 days after irradiation, the number of foci rose quickly and leveled off between Day 19 and Day 23. This late appearance of the IAP-positive foci suggested that the neoplastic transformation process was not an immediate consequence of radiation damage. The mechanism underlying this observation was unknown. The possibility existed that very small foci and/or foci expressing a low level of IAP were being missed at earlier expression times. The increased sensitivity of the WB staining technique has allowed for the reinvestigation of the kinetics of induction of radiation-induced foci in this system. Experiments were performed where parallel groups of transformation flasks were stained at Days 7, 9, 11, 13, 15, 17, 19, and 21 days after irradiation. The data clearly indicate that the radiation induction of IAP-positive foci is indeed delayed in this system with the vast majority of the foci beginning to appear after Day 9 after irradiation. The delay is not the result of a lack of ability to detect small IAP-positive foci since foci with as few as 15 IAP-positive cells were discernible. We have reported previously that under identical experimental conditions both the establishment of plateau phase and the onset of the expression of lethal mutations also occur after Day 9. We therefore propose that radiation-induced neoplastic transformation of HeLa x skin fibroblast hybrid cells is a consequence of the delayed expression of heritable damage under epigenetic control with a resultant loss of tumor-suppressor function.

Original languageEnglish (US)
Pages (from-to)209-216
Number of pages8
JournalRadiation Research
Volume134
Issue number2
DOIs
StatePublished - 1993
Externally publishedYes

Fingerprint

Hybrid Cells
Epigenomics
epigenetics
phosphatases
Alkaline Phosphatase
alkaline phosphatase
Radiation
damage
radiation
cells
staining
irradiation
Staining and Labeling
fibroblasts
antibodies
Fibroblasts
induction
Neoplastic Processes
Chromogenic Compounds
tumors

ASJC Scopus subject areas

  • Agricultural and Biological Sciences (miscellaneous)
  • Radiology Nuclear Medicine and imaging
  • Biophysics
  • Radiation

Cite this

Delayed heritable damage and epigenetics in radiation-induced neoplastic transformation of human hybrid cells. / Mendonca, Marc; Antoniono, R. J.; Redpath, J. L.

In: Radiation Research, Vol. 134, No. 2, 1993, p. 209-216.

Research output: Contribution to journalArticle

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