YEN-SHEN LUHUANG-CHUN LIENYeh P.-Y.KUN-HUEI YEHKuo M.-L.SUNG-HSIN KUOANN-LII CHENG2021-09-012021-09-0120051007-9327https://www.scopus.com/inward/record.uri?eid=2-s2.0-29544451180&doi=10.3748%2fwjg.v11.i40.6373&partnerID=40&md5=55c4852897951f62c5fde21ce383ebf0https://scholars.lib.ntu.edu.tw/handle/123456789/580383Aim: To determine how glucocorticoids (GCs) may affect the growth and chemosensitivity of common carcinoma cells. Methods: The effect of dexamethasone (DEX) on growth and chemosensitivity was assessed in 14 carcinoma cell lines. The function of GC receptors (GR) was assessed by MMTV reporter assay. Overexpression of GR was done by in vitro transfection and expression of a GR-expressing vector. Immunohistochemical stain of tissues and cells were done by PA1-511A, an anti-GR monoclonal antibody. Results: DEX inhibited cell growth of four (MCF-7, MCF-7/MXR1, MCF-7/TPT300, and HeLa), increased cisplatin cytotoxicity of one (SiHa), and decreased cisplatin cytotoxicity of two (H460 and Hep3B) cell lines. The GR content of the seven cell lines affected by DEX was significantly higher than those of the seven cell lines unaffected by DEX (5.2±2.5×104 sites/cell vs 1.3±1.4×104 sites/cell, P= 0.005). Only two DEX-unresponsive cell lines (NPC-TWO1 and NPC-TWO4) contained high GR amounts in the range (1.9-8.1 × 104 sites/cell) of the seven DEX-responsive cell lines. The GR function of NPC-TWO1 and NPC-TWO4, however, was found to be impaired. The importance of high cellular amount of GR in mediating DEX susceptibility of the cells was further exemplified by GR dose-dependent drug resistance to cisplatin of AGS, a cell line with low GR content and was unaffected by DEX before transfection of GR-expressing vector. Immunohistochemical studies of human cancer tissues showed that 5 of the 45 (11.1%) breast cancer and 43 of the 85 (50.6%) non-small cell lung cancer had high GR contents at the ranges of the GC-responsive carcinoma cell lines. Conclusion: The growth and chemosensitivity of human carcinomas with high GR contents may be affected by GC. However, in light of the heterogeneous and even contradictive effects of GC on these cells, routine examination of GR contents of human carcinoma tissues may not be clinically useful until other markers that help predict the ultimate effect of GC on individual patients are identified. ? 2005 The WJG Press and Elsevier Inc. All rights reserved.[SDGs]SDG3cisplatin; dexamethasone; glucocorticoid; glucocorticoid receptor; article; breast cancer; cancer cell culture; cancer growth; cancer inhibition; carcinoma; carcinoma cell; cell heterogeneity; chemosensitivity; controlled study; cytotoxicity; drug efficacy; drug receptor binding; drug sensitivity; enzyme linked immunosorbent assay; expression vector; gene overexpression; histopathology; human; human cell; human tissue; immunohistochemistry; in vitro study; lung carcinoma; lung non small cell cancer; protein expression; protein function; reporter gene; statistical significance; uterine cervix carcinomajournal article10.3748/wjg.v11.i40.6373164191682-s2.0-29544451180