Literature DB >> 1988112

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

R Grundel1, H Rubin.   

Abstract

Confluence is an agent that promotes the progressive acquisition of the focus forming phenotype in clones of cells within NIH-3T3 populations. This conclusion is based on four results. (a) Even in cultures which have been confluent for more than 2 weeks without making foci, some cells in those cultures have been affected by the confluent state and will make foci if replated and allowed to grow into new saturated cultures. Because replicate dishes are very similar in the number and type of foci formed after replating, we conclude that the progression toward focus formation is substantially completed before replating, while the cells are in their original confluent cultures. (b) Different NIH-3T3 populations were produced by expansion of small or large numbers of starting cells. When plated without exposure to confluence there was little difference in focus production among cells from these different sized starter populations. However, confluence caused foci to arise more frequently in platings of 10(5) cells derived from large starting numbers than from platings of 10(5) cells derived from small starting numbers of cells. This implies that the confluent state successfully promotes the acquisition of the focus forming phenotype in a limited percentage of cells in an NIH-3T3 culture and that those cells are absent from many small starting populations. (c) There is a progressive temporal effect of the confluent state on focus formation; the number and density of foci that emerge from replated confluent cultures increase with the length of time the cells spend in the confluent state. (d) There is heterogeneity among different batches of NIH-3T3 cells in the ability of the confluent state to induce acquisition of the focus forming phenotype. Also, the morphology of the foci that do arise after confluent treatment differs substantially among cell populations. Nonetheless, the foci formed from a single batch of cells are typically similar in morphology, indicating that those foci arose from one clone, or very few clones, of cells.

Mesh:

Year:  1991        PMID: 1988112

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  9 in total

1.  Clonal dynamics of progressive neoplastic transformation.

Authors:  M Chow; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

Review 2.  A free-radical hypothesis for the instability and evolution of genotype and phenotype in vitro.

Authors:  R E Parchment; K Natarajan
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

3.  High rate of diversification and reversal among subclones of neoplastically transformed NIH 3T3 clones.

Authors:  A L Rubin; A Sneade-Koenig; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-01       Impact factor: 11.205

4.  Growth in high serum concentrations leads to rapid deadaptation of cells previously adapted to growth in an extremely low concentration of serum.

Authors:  A Yao; W Huang; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

Review 5.  Technical considerations for studying cancer metastasis in vivo.

Authors:  D R Welch
Journal:  Clin Exp Metastasis       Date:  1997-05       Impact factor: 5.150

Review 6.  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

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

Authors:  M Chow; A Yao; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1994-01-18       Impact factor: 11.205

8.  Promotion and selection by serum growth factors drive field cancerization, which is anticipated in vivo by type 2 diabetes and obesity.

Authors:  Harry Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-01       Impact factor: 11.205

9.  Sensitivity of transformation to small differences in population density during serial passage of NIH 3T3 cells.

Authors:  A Yao; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

  9 in total

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