Alteration of Telomere Length in Lung Cancer
There are characteristic G-rich repeats, i.e. telomeric repeats, at every chromosome end in eukaryotes. Telomeres are thought to protect chromosomes from end-to-end fusion or exonucleolytic degradation. Stabilization of telomeres is considered to be concomitant with the attainment of immortality in...
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Veröffentlicht in: | Haigan 1997/04/20, Vol.37(2), pp.189-195 |
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description | There are characteristic G-rich repeats, i.e. telomeric repeats, at every chromosome end in eukaryotes. Telomeres are thought to protect chromosomes from end-to-end fusion or exonucleolytic degradation. Stabilization of telomeres is considered to be concomitant with the attainment of immortality in tumor cells. Using the Southern blotting method, we examined telomere length in 71 surgically resected primary lung cancer tissues and adjacent noncancerous tissues. Among 71 primary lung cancer tissues, alterations in telomere length were observed in 19 tumors (26.8%) including 13 with short and 6 with elongated telomeres. Alterations of telomere length were frequently observed in small cell carcinomas and tumors with high levels of telomerase activity. The present results indicate that the proliferative potential of lung cancer cells is likely to be more affected by histology and genetic alterations than clinical stage. |
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The present results indicate that the proliferative potential of lung cancer cells is likely to be more affected by histology and genetic alterations than clinical stage.</description><subject>Immortalization</subject><subject>Lung cancer</subject><subject>Telomerase</subject><subject>Telomere</subject><issn>0386-9628</issn><issn>1348-9992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNo9j0tLw0AUhQdRMFaX7vMDTJ1HMjN3WYJVIeCmroeb5OZR0olM4sJ_b0pKN_fA5TsHPsaeBd_K1MrXDvsW_VaZrbBwwyKhUpsAgLxlEVdWJ6ClvWcP03TkXMtMq4i97IaZAs796OOxiQ80jCcKFBfk27mLex8Xv76Nc_QVhUd21-Aw0dMlN-x7_3bIP5Li6_0z3xVJJXUGiSSwuhQNEgqhMEWQBsrGZLqWRhjUskwtaTCVAsG1xrLGGlSqiHMUy3fDknW3CuM0BWrcT-hPGP6c4O6s6lZVp4xbVBd-v_LHacaWrjSGua8GutACND835HqW4hWoOgyOvPoHsWxfxQ</recordid><startdate>1997</startdate><enddate>1997</enddate><creator>Shirotani, Yoshifumi</creator><general>The Japan Lung Cancer Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1997</creationdate><title>Alteration of Telomere Length in Lung Cancer</title><author>Shirotani, Yoshifumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2659-2e986b1faea113a4a9279bf756d2717a62b48e697c391066abdad9343e00a17c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1997</creationdate><topic>Immortalization</topic><topic>Lung cancer</topic><topic>Telomerase</topic><topic>Telomere</topic><toplevel>online_resources</toplevel><creatorcontrib>Shirotani, Yoshifumi</creatorcontrib><collection>CrossRef</collection><jtitle>Haigan</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shirotani, Yoshifumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alteration of Telomere Length in Lung Cancer</atitle><jtitle>Haigan</jtitle><addtitle>JJLC</addtitle><date>1997</date><risdate>1997</risdate><volume>37</volume><issue>2</issue><spage>189</spage><epage>195</epage><pages>189-195</pages><issn>0386-9628</issn><eissn>1348-9992</eissn><abstract>There are characteristic G-rich repeats, i.e. telomeric repeats, at every chromosome end in eukaryotes. Telomeres are thought to protect chromosomes from end-to-end fusion or exonucleolytic degradation. Stabilization of telomeres is considered to be concomitant with the attainment of immortality in tumor cells. Using the Southern blotting method, we examined telomere length in 71 surgically resected primary lung cancer tissues and adjacent noncancerous tissues. Among 71 primary lung cancer tissues, alterations in telomere length were observed in 19 tumors (26.8%) including 13 with short and 6 with elongated telomeres. Alterations of telomere length were frequently observed in small cell carcinomas and tumors with high levels of telomerase activity. The present results indicate that the proliferative potential of lung cancer cells is likely to be more affected by histology and genetic alterations than clinical stage.</abstract><pub>The Japan Lung Cancer Society</pub><doi>10.2482/haigan.37.189</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Immortalization Lung cancer Telomerase Telomere |
title | Alteration of Telomere Length in Lung Cancer |
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