Literature DB >> 27939322

Two populations of TSPO binding sites in oral cancer SCC-15 cells.

Avishai Gavish1, Ella Krayzler2, Rafael Nagler3.   

Abstract

Oral cancer mortality and morbidity rates remain high. The main inducer of oral cancer is cigarette smoke (CS). Translocator protein 18kDa (TSPO) was shown to play a role in carcinogenesis. We characterized TSPO binding sites in human oral cancer cell line SCC-15 and examined effect of CS on TSPO binding. We exposed SCC-15 human squamous cells to cigarette smoke. [3H]PK 11195 binding results were assessed in cells confluent for one day. To characterize the number of population sites, a custom written Matlab program compared Pearson linear correlation coefficients between all points in the Scatchard plot. Using [3H]PK 11195 as a radio ligand, we found that TSPO binding sites are not uniform, but separated into two sub-populations, one with high affinity (respective Kd and Bmax values of 1.40±0.08nM and 1586±48 fmol/mg protein), another with lower affinity (respective Kd and Bmax values of 61±5nM and 26260±1050 fmol/mg protein). We demonstrate rapid decrease in TSPO binding to the high affinity site induced by exposure to CS; specifically, significant 36% decrease in binding after 30min CS exposure (p<0.05), and 69% decrease after 2h CS exposure (p<0.05). Association between TSPO and CS exposure may contribute to understanding the underlying mechanism of oral carcinogenesis.
Copyright © 2016. Published by Elsevier Inc.

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Keywords:  Cigarette smoke; SCC-15 oral cancer cell line; Translocator protein 18kDa (TSPO); [(3)H]PK 11195

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Year:  2016        PMID: 27939322     DOI: 10.1016/j.yexcr.2016.12.005

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  1 in total

1.  Pathway-focused PCR array profiling of CAL-27 cell with over-expressed ZNF750.

Authors:  Li Pan; Hongli Yang; Wenqiang Tang; Cong Xu; Shuangfeng Chen; Zhen Meng; Keyi Li; Haiying Chen
Journal:  Oncotarget       Date:  2017-12-09
  1 in total

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