Literature DB >> 8290570

Cellular epigenetics: topochronology of progressive "spontaneous" transformation of cells under growth constraint.

M Chow1, A Yao, H Rubin.   

Abstract

Early passages of NIH 3T3 cells yield about 10 transformed foci for every 10(5) cells seeded after the cells multiply to confluence in a standardized 2-week assay. The question arose whether more cells would give rise to foci if given more time for their development. This question could not be answered simply by extending the incubation period, since the original foci spread to cover much of the area of the culture dish. Transformed cells can also detach into the medium from the original foci to initiate new foci by reattaching at a distance. These problems were averted by growing cells in multiwell plates which in effect simulated partitioned culture dishes. All the wells in a given plate were assayed for focus formation at successive intervals up to 14 weeks. The results indicated the spatial pattern and sequence of transformation on different parts of the "partitioned" dish. The number of multiwells containing focus-forming cells increased steadily with time, indicating that all parts of a dish eventually undergo transformation. Also, most of the transformations were recorded long after confluence in the multiwells was reached. Hence such a transformation is much more likely to occur in the nondividing state rather than in the dividing state of the cells and is thus inconsistent with a mutational basis. The results suggest that "spontaneous" transformation is a population-wide, epigenetic phenomenon. This agrees with the results from clonal analysis and other studies and is well described by the concept of progressive state selection, in which "spontaneous" transformation represents a heterogeneous, adaptive response of competent cells to moderate constraints on cell growth.

Mesh:

Year:  1994        PMID: 8290570      PMCID: PMC42996          DOI: 10.1073/pnas.91.2.599

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  11 in total

1.  Physiological induction and reversal of focus formation and tumorigenicity in NIH 3T3 cells.

Authors:  A L Rubin; P Arnstein; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

2.  Progressive state selection of cells in low serum promotes high density growth and neoplastic transformation in NIH 3T3 cells.

Authors:  A Yao; A L Rubin; H Rubin
Journal:  Cancer Res       Date:  1990-08-15       Impact factor: 12.701

3.  Relation of spontaneous transformation in cell culture to adaptive growth and clonal heterogeneity.

Authors:  A L Rubin; A Yao; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

4.  Effect of interclonal heterogeneity on the progressive, confluence-mediated acquisition of the focus-forming phenotype in NIH-3T3 populations.

Authors:  R Grundel; H Rubin
Journal:  Cancer Res       Date:  1991-02-01       Impact factor: 12.701

5.  Relationship between x-ray exposure and malignant transformation in C3H 10T1/2 cells.

Authors:  A R Kennedy; M Fox; G Murphy; J B Little
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

6.  Improved medium and culture conditions for clonal growth with minimal serum protein and for enhanced serum-free survival of Swiss 3T3 cells.

Authors:  G D Shipley; R G Ham
Journal:  In Vitro       Date:  1981-08

7.  In vitro malignant transformation by methylcholanthrene of the progeny of single cells derived from C3H mouse prostate.

Authors:  S Mondal; C Heidelberger
Journal:  Proc Natl Acad Sci U S A       Date:  1970-01       Impact factor: 11.205

8.  Evidence for the progressive and adaptive nature of spontaneous transformation in the NIH 3T3 cell line.

Authors:  H Rubin; K Xu
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

9.  Emergence of neoplastic transformants spontaneously or after exposure to N-methyl-N'-nitro-N-nitrosoguanidine in populations of rat liver epithelial cells cultured under selective and nonselective conditions.

Authors:  L W Lee; M S Tsao; J W Grisham; G J Smith
Journal:  Am J Pathol       Date:  1989-07       Impact factor: 4.307

10.  Murine sarcoma and leukemia viruses: assay using clonal lines of contact-inhibited mouse cells.

Authors:  J L Jainchill; S A Aaronson; G J Todaro
Journal:  J Virol       Date:  1969-11       Impact factor: 5.103

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  4 in total

1.  Relation of the slow growth phenotype to neoplastic transformation: possible significance for human cancer.

Authors:  M Chow; H Rubin
Journal:  In Vitro Cell Dev Biol Anim       Date:  1999-09       Impact factor: 2.416

Review 2.  Phenotypic selection as the biological mode of epigenetic conversion and reversion in cell transformation.

Authors:  Harry Rubin; Andrew L Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-08       Impact factor: 11.205

3.  Heritable, population-wide damage to cells as the driving force of neoplastic transformation.

Authors:  H Rubin; A Yao; M Chow
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-23       Impact factor: 11.205

4.  Cellular epigenetics: control of the size, shape, and spatial distribution of transformed foci by interactions between the transformed and nontransformed cells.

Authors:  H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-01       Impact factor: 11.205

  4 in total

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