A nonrandom chromosomal abnormality, del 3p(14-23), in human small cell lung cancer (SCLC)

J. Whang-Peng, P. A. Bunn, C. S. Kao-Shan, E. C. Lee, D. N. Carney, A. Gazdar, J. D. Minna

研究成果: 雜誌貢獻文章

293 引文 (Scopus)

摘要

In order to determine whether or not there are specific chromosomal changes in small cell lung cancer (SCLC), karyotypic analyses of 16 continuous SCLC tissue culture lines, three fresh tumor specimens (bone marrow), one direct preparation of bone marrow involved with SCLC, and two lymphoblastoid lines derived from SCLC patients were studied. Cell lines were derived from primary tumor, or metastases to bone marrow, subcutaneous nodules, or pleural fluid; all 16 lines had biochemical and histologic proporties characteristic of SCLC. Of the 15 males and 3 females, 6 patients had no prior treatment. All of the 16 cell lines, the 3 fresh specimens, and the direct bone marrow preparation had a common deletion of the short arm of chromosome #3. Use of the shortest region of overlap analysis showed the common deletion was of the short arm in the regions p(14-23). This specific chromosomal abnormality, del 3p, was not found in five non-SCLC cell lines studied and is of major potential biological and diagnostic importance.
原文英語
頁(從 - 到)119-134
頁數16
期刊Cancer Genetics and Cytogenetics
6
發行號2
DOIs
出版狀態已發佈 - 一月 1 1982
對外發佈Yes

指紋

Small Cell Lung Carcinoma
Chromosome Aberrations
Bone Marrow
Cell Line
Chromosomes, Human, Pair 3
Non-Small Cell Lung Carcinoma
Neoplasms
Neoplasm Metastasis

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

引用此文

A nonrandom chromosomal abnormality, del 3p(14-23), in human small cell lung cancer (SCLC). / Whang-Peng, J.; Bunn, P. A.; Kao-Shan, C. S.; Lee, E. C.; Carney, D. N.; Gazdar, A.; Minna, J. D.

於: Cancer Genetics and Cytogenetics, 卷 6, 編號 2, 01.01.1982, p. 119-134.

研究成果: 雜誌貢獻文章

Whang-Peng, J. ; Bunn, P. A. ; Kao-Shan, C. S. ; Lee, E. C. ; Carney, D. N. ; Gazdar, A. ; Minna, J. D. / A nonrandom chromosomal abnormality, del 3p(14-23), in human small cell lung cancer (SCLC). 於: Cancer Genetics and Cytogenetics. 1982 ; 卷 6, 編號 2. 頁 119-134.
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AU - Bunn, P. A.

AU - Kao-Shan, C. S.

AU - Lee, E. C.

AU - Carney, D. N.

AU - Gazdar, A.

AU - Minna, J. D.

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N2 - In order to determine whether or not there are specific chromosomal changes in small cell lung cancer (SCLC), karyotypic analyses of 16 continuous SCLC tissue culture lines, three fresh tumor specimens (bone marrow), one direct preparation of bone marrow involved with SCLC, and two lymphoblastoid lines derived from SCLC patients were studied. Cell lines were derived from primary tumor, or metastases to bone marrow, subcutaneous nodules, or pleural fluid; all 16 lines had biochemical and histologic proporties characteristic of SCLC. Of the 15 males and 3 females, 6 patients had no prior treatment. All of the 16 cell lines, the 3 fresh specimens, and the direct bone marrow preparation had a common deletion of the short arm of chromosome #3. Use of the shortest region of overlap analysis showed the common deletion was of the short arm in the regions p(14-23). This specific chromosomal abnormality, del 3p, was not found in five non-SCLC cell lines studied and is of major potential biological and diagnostic importance.

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