Literature DB >> 2553086

Small cell lung cancer cell lines secrete predominantly ACTH precursor peptides not ACTH.

M F Stewart1, S R Crosby, S Gibson, P R Twentyman, A White.   

Abstract

A panel of 18 well characterised human small cell lung cancer (SCLC) cell lines was assessed for the production of adrenocorticotrophin (ACTH) and its precursor peptides, pro-opiomelanocortin (POMC) and pro-ACTH. These precursor peptides were measured directly using a novel two-site immunoradiometric assay (IRMA) based on monoclonal antibodies, in conjunction with a similar IRMA for ACTH 1-39. Significant concentrations of ACTH precursors were secreted by 10 of the 18 cell lines (56%). The low levels of ACTH immunoreactivity detected in seven cell lines could be accounted for by the known cross-reactivity of precursors in the ACTH IRMA. This suggests there is little, if any, processing of ACTH precursors to ACTH. Cell pellet extracts contained undetectable or low levels of ACTH precursors and ACTH, indicating that these peptides are not stored intracellularly. During the growth of the SCLC cells in vitro ACTH precursors accumulated progressively in the culture medium. Thus the combination of a direct assay for the ACTH precursors and the panel of SCLC cell lines provides a valuable in vitro model for the expression of POMC in human tumours.

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Year:  1989        PMID: 2553086      PMCID: PMC2247354          DOI: 10.1038/bjc.1989.212

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  20 in total

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Authors:  G Bepler; D N Carney; A F Gazdar; J D Minna
Journal:  Cancer Res       Date:  1987-05-01       Impact factor: 12.701

2.  Characterization of three new variant type cell lines derived from small cell carcinoma of the lung.

Authors:  L de Leij; P E Postmus; C H Buys; J D Elema; F Ramaekers; S Poppema; M Brouwer; A Y van der Veen; G Mesander; T H The
Journal:  Cancer Res       Date:  1985-12       Impact factor: 12.701

3.  Peptide hormone production in primary lung tumors.

Authors:  K Yamaguchi; K Abe; I Adachi; S Kimura; M Suzuki; A Shimada; T Kodama; T Kameya; Y Shimosato
Journal:  Recent Results Cancer Res       Date:  1985

4.  A simplified in situ solubilization procedure for the determination of DNA and cell number in tissue cultured mammalian cells.

Authors:  D C West; A Sattar; S Kumar
Journal:  Anal Biochem       Date:  1985-06       Impact factor: 3.365

5.  Stimulation of adrenal mitogenesis by N-terminal proopiocortin peptides.

Authors:  F E Estivariz; F Iturriza; C McLean; J Hope; P J Lowry
Journal:  Nature       Date:  1982-06-03       Impact factor: 49.962

6.  Peptide hormone production in lung cancer cell lines of different histopathological types.

Authors:  W Luster; C Gropp; H F Kern; R Wahl; H D Röher; K Havemann
Journal:  Recent Results Cancer Res       Date:  1985

7.  Clinical evaluation of a two-site immunoradiometric assay for adrenocorticotrophin in unextracted human plasma using monoclonal antibodies.

Authors:  A White; H Smith; M Hoadley; S H Dobson; J G Ratcliffe
Journal:  Clin Endocrinol (Oxf)       Date:  1987-01       Impact factor: 3.478

8.  Establishment and identification of small cell lung cancer cell lines having classic and variant features.

Authors:  D N Carney; A F Gazdar; G Bepler; J G Guccion; P J Marangos; T W Moody; M H Zweig; J D Minna
Journal:  Cancer Res       Date:  1985-06       Impact factor: 12.701

9.  Characterization of pro-opiomelanocortin-derived peptides in pituitary and ectopic adrenocorticotrophin-secreting tumours.

Authors:  A C Hale; G M Besser; L H Rees
Journal:  J Endocrinol       Date:  1986-01       Impact factor: 4.286

10.  Establishment and characterisation of cell lines from patients with lung cancer (predominantly small cell carcinoma).

Authors:  H Baillie-Johnson; P R Twentyman; N E Fox; G A Walls; P Workman; J V Watson; N Johnson; J G Reeve; N M Bleehen
Journal:  Br J Cancer       Date:  1985-10       Impact factor: 7.640

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3.  The tobacco carcinogen NNK drives accumulation of DNMT1 at the GR promoter thereby reducing GR expression in untransformed lung fibroblasts.

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