| Literature DB >> 33466597 |
Claudia Musial1, Renata Zaucha2, Alicja Kuban-Jankowska1, Lucyna Konieczna3, Mariusz Belka3, Antonella Marino Gammazza4, Tomasz Baczek3, Francesco Cappello4, Michal Wozniak1, Magdalena Gorska-Ponikowska1.
Abstract
Malignant neoplasms are among the most common diseases and are responsible for the majority of deaths in the developed world. In contrast to men, available data show a clear upward trend in the incidence of lung cancer in women, making it almost as prevalent as breast cancer. Women might be more susceptible to the carcinogenic effect of tobacco smoke than men. Furthermore, available data indicate a much more frequent mutation of the tumor suppressor gene-p53 in non-small cell lung cancer (NSCLC) female patients compared to males. Another important factor, however, might lie in the female sex hormones, whose mitogenic or carcinogenic effect is well known. Epidemiologic data show a correlation between hormone replacement therapy (HRT) or oral contraceptives (OCs), and increased mortality rates due to the increased incidence of malignant tumors, including lung cancer. Interestingly, two types of estrogen receptors have been detected in lung cancer cells: ERα and ERβ. The presence of ERα has been detected in tissues and non-small-cell lung carcinoma (NSCLC) cell lines. In contrast, overexpression of ERβ is a prognostic marker in NSCLC. Herein, we summarize the current knowledge on the role of estrogens in the etiopathogenesis of lung cancer, as well as biological, hormonal and genetic sex-related differences in this neoplasm.Entities:
Keywords: 17β-estradiol; A549; NSCLC; estrogen receptor; estrogens; lung adenocarcinoma; lung cancer; non-small cell lung cancer; p53; sex hormones
Year: 2021 PMID: 33466597 PMCID: PMC7828659 DOI: 10.3390/ijerph18020648
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390