Cellular Epigenetics: Topochronology of Progressive "Spontaneous" Transformation of Cells Under Growth Constraint

Early passages of NIH 3T3 cells yield about 10 transformed foci for every 105cells 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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1994-01, Vol.91 (2), p.599-603
Hauptverfasser: Chow, Ming, Yao, Adam, Rubin, Harry
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 603
container_issue 2
container_start_page 599
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 91
creator Chow, Ming
Yao, Adam
Rubin, Harry
description Early passages of NIH 3T3 cells yield about 10 transformed foci for every 105cells 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.
doi_str_mv 10.1073/pnas.91.2.599
format Article
fullrecord <record><control><sourceid>jstor_pnas_</sourceid><recordid>TN_cdi_jstor_primary_2363931</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>2363931</jstor_id><sourcerecordid>2363931</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4609-17fa721eebfde9f519aa7076e889fe7d28aa470798a9e6f2e39b2290807d441d3</originalsourceid><addsrcrecordid>eNp9kcFv0zAUxi3ENMrgyA2kqNK4pTzbaRwjLqga26RJINGdLTd5blOldmY7Y_vvcdSuAw6cLL3v9z2_Tx8h7yjMKAj-qbc6zCSdsdlcyhdkQkHSvCwkvCQTACbyqmDFK_I6hC0AyHkFp-S0YhLmAibkboFdN3TaZxd9u0aLsa3D52zpeldvvLOuc-vHzJnsh3drjyG095hNf_bORm3RDWGaLb22wTi_07F1dmTHnSG7tQ367NK7X3GTLZwN0evWxjfkxOgu4NvDe0Zuv10sF1f5zffL68XXm7wuSpA5FUYLRhFXpkFp5lRqLUCUWFXSoGhYpXWRBrLSEkvDkMsVS6kqEE1R0IafkS_7vf2w2mFTo03_d6r37U77R-V0q_5WbLtRa3evCiZlmewfD3bv7gYMUe3aUKdg-9hKlJxXXEICp_-AWzd4m6IpBpRTwWGE8j1UexeCR3O8g4Iaa1RjjUpSxVSqMfEf_jz-SB96S_r5QR9tT-qTXZmh6yI-xMS9_w_3LG9DdP6oM15yySn_DZT_vD4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>201317300</pqid></control><display><type>article</type><title>Cellular Epigenetics: Topochronology of Progressive "Spontaneous" Transformation of Cells Under Growth Constraint</title><source>MEDLINE</source><source>JSTOR Archive Collection A-Z Listing</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Chow, Ming ; Yao, Adam ; Rubin, Harry</creator><creatorcontrib>Chow, Ming ; Yao, Adam ; Rubin, Harry</creatorcontrib><description>Early passages of NIH 3T3 cells yield about 10 transformed foci for every 105cells 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.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.91.2.599</identifier><identifier>PMID: 8290570</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>3T3 cells ; 3T3 Cells - pathology ; Animals ; Cell Division ; Cell growth ; Cell lines ; Cell Transformation, Neoplastic ; Cells ; Cellular biology ; Cultured cells ; Epigenetics ; Epithelial cells ; Mice ; NIH 3T3 cells ; Phenotype ; Seeding ; Time Factors ; Transformed cell line ; Tumors</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1994-01, Vol.91 (2), p.599-603</ispartof><rights>Copyright 1994 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Jan 18, 1994</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4609-17fa721eebfde9f519aa7076e889fe7d28aa470798a9e6f2e39b2290807d441d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/91/2.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2363931$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2363931$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8290570$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chow, Ming</creatorcontrib><creatorcontrib>Yao, Adam</creatorcontrib><creatorcontrib>Rubin, Harry</creatorcontrib><title>Cellular Epigenetics: Topochronology of Progressive "Spontaneous" Transformation of Cells Under Growth Constraint</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Early passages of NIH 3T3 cells yield about 10 transformed foci for every 105cells 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.</description><subject>3T3 cells</subject><subject>3T3 Cells - pathology</subject><subject>Animals</subject><subject>Cell Division</subject><subject>Cell growth</subject><subject>Cell lines</subject><subject>Cell Transformation, Neoplastic</subject><subject>Cells</subject><subject>Cellular biology</subject><subject>Cultured cells</subject><subject>Epigenetics</subject><subject>Epithelial cells</subject><subject>Mice</subject><subject>NIH 3T3 cells</subject><subject>Phenotype</subject><subject>Seeding</subject><subject>Time Factors</subject><subject>Transformed cell line</subject><subject>Tumors</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFv0zAUxi3ENMrgyA2kqNK4pTzbaRwjLqga26RJINGdLTd5blOldmY7Y_vvcdSuAw6cLL3v9z2_Tx8h7yjMKAj-qbc6zCSdsdlcyhdkQkHSvCwkvCQTACbyqmDFK_I6hC0AyHkFp-S0YhLmAibkboFdN3TaZxd9u0aLsa3D52zpeldvvLOuc-vHzJnsh3drjyG095hNf_bORm3RDWGaLb22wTi_07F1dmTHnSG7tQ367NK7X3GTLZwN0evWxjfkxOgu4NvDe0Zuv10sF1f5zffL68XXm7wuSpA5FUYLRhFXpkFp5lRqLUCUWFXSoGhYpXWRBrLSEkvDkMsVS6kqEE1R0IafkS_7vf2w2mFTo03_d6r37U77R-V0q_5WbLtRa3evCiZlmewfD3bv7gYMUe3aUKdg-9hKlJxXXEICp_-AWzd4m6IpBpRTwWGE8j1UexeCR3O8g4Iaa1RjjUpSxVSqMfEf_jz-SB96S_r5QR9tT-qTXZmh6yI-xMS9_w_3LG9DdP6oM15yySn_DZT_vD4</recordid><startdate>19940118</startdate><enddate>19940118</enddate><creator>Chow, Ming</creator><creator>Yao, Adam</creator><creator>Rubin, Harry</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19940118</creationdate><title>Cellular Epigenetics: Topochronology of Progressive "Spontaneous" Transformation of Cells Under Growth Constraint</title><author>Chow, Ming ; Yao, Adam ; Rubin, Harry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4609-17fa721eebfde9f519aa7076e889fe7d28aa470798a9e6f2e39b2290807d441d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>3T3 cells</topic><topic>3T3 Cells - pathology</topic><topic>Animals</topic><topic>Cell Division</topic><topic>Cell growth</topic><topic>Cell lines</topic><topic>Cell Transformation, Neoplastic</topic><topic>Cells</topic><topic>Cellular biology</topic><topic>Cultured cells</topic><topic>Epigenetics</topic><topic>Epithelial cells</topic><topic>Mice</topic><topic>NIH 3T3 cells</topic><topic>Phenotype</topic><topic>Seeding</topic><topic>Time Factors</topic><topic>Transformed cell line</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chow, Ming</creatorcontrib><creatorcontrib>Yao, Adam</creatorcontrib><creatorcontrib>Rubin, Harry</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chow, Ming</au><au>Yao, Adam</au><au>Rubin, Harry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular Epigenetics: Topochronology of Progressive "Spontaneous" Transformation of Cells Under Growth Constraint</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1994-01-18</date><risdate>1994</risdate><volume>91</volume><issue>2</issue><spage>599</spage><epage>603</epage><pages>599-603</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Early passages of NIH 3T3 cells yield about 10 transformed foci for every 105cells 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.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>8290570</pmid><doi>10.1073/pnas.91.2.599</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0027-8424
ispartof Proceedings of the National Academy of Sciences - PNAS, 1994-01, Vol.91 (2), p.599-603
issn 0027-8424
1091-6490
language eng
recordid cdi_jstor_primary_2363931
source MEDLINE; JSTOR Archive Collection A-Z Listing; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects 3T3 cells
3T3 Cells - pathology
Animals
Cell Division
Cell growth
Cell lines
Cell Transformation, Neoplastic
Cells
Cellular biology
Cultured cells
Epigenetics
Epithelial cells
Mice
NIH 3T3 cells
Phenotype
Seeding
Time Factors
Transformed cell line
Tumors
title Cellular Epigenetics: Topochronology of Progressive "Spontaneous" Transformation of Cells Under Growth Constraint
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T20%3A38%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_pnas_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cellular%20Epigenetics:%20Topochronology%20of%20Progressive%20%22Spontaneous%22%20Transformation%20of%20Cells%20Under%20Growth%20Constraint&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Chow,%20Ming&rft.date=1994-01-18&rft.volume=91&rft.issue=2&rft.spage=599&rft.epage=603&rft.pages=599-603&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.91.2.599&rft_dat=%3Cjstor_pnas_%3E2363931%3C/jstor_pnas_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=201317300&rft_id=info:pmid/8290570&rft_jstor_id=2363931&rfr_iscdi=true