Cigarette smoke upregulates Notch-1 signaling pathway and promotes lung adenocarcinoma progression. (1st February 2022)

• Record Type: Journal Article
• Authors: Chiappara, Giuseppina; Di Vincenzo, Serena; Sangiorgi, Claudia; Di Sano, Caterina; D'Anna, Claudia; Zito, Giovanni; Cipollina, Chiara; Vitulo, Patrizio; Bertani, Alessandro; Pace, Elisabetta
• Is Part Of: Toxicology letters. Volume 355(2022)
• Page Start: 31
• Page End: 40
• Publication Date: 2022-02-01
• Subjects: Cigarette smoke -- Lung adenocarcinoma -- Notch-1 -- Cancer progression; Toxicology -- Periodicals; 363.179
• DOI: 10.1016/j.toxlet.2021.11.002
• Languages: English
• ISSNs: 0378-4274

Abstract

Highlights: Notch-1 pathway plays an important role in lung carcinoma. Lung parenchyma from Smokers exhibited higher expression of Notch-1. CSE increases Notch-1 activation and Hes-1 target gene in lung cancer cells. Notch-1 modulation affects ki-67 and survivin expression in lung cancer cells. Abstract: Notch-1 pathway plays an important role in lung carcinoma, stem cell regulation, cellular communication, growth and differentiation. Cigarette smoke is involved in the regulation of Notch signaling. However, current data regarding the impact of cigarette smoke on the Notch pathway in lung cancer progression are limited. The present study aimed to explore whether cigarette smoke exposure altered Notch-1 pathway in ex-vivo (surgical samples of lung parenchyma from non-smoker and smoker patients with lung adenocarcinoma) and in vitro (adenocarcinoma A549 cell line) approaches. The expression of Notch-1, Jagged-1 and CD133 in surgical samples was evaluated by immunohistochemistry. A549 were exposed to cigarette smoke extracts (2.5 % and 5 % CSE for 6, 24 and 48 h) and the expression of Notch-1, Jagged-1 and Hes-1 was evaluated by Real-Time PCR and Western Blot (nuclear fractions). Expression and localization of Notch-1, Hes-1, CD133 and ABCG2 were assessed by immunofluorescence. The expression of survivin and Ki-67 was assessed by flow cytometry following CSE exposure and inhibition of Notch-1 signaling. Smokers lung parenchyma exhibited higher expression of Notch-1. CSE exposure increased Notch-1 and Hes-1 gene and nuclear protein expression in A549. Immunofluorescence confirmed higher expression of nuclear Hes-1 in CSE-stimulated A549 cells. CSE increased both survivin and Ki-67 expression and this effect was reverted by inhibition of the Notch-1 pathway. In conclusion, these data show that cigarette smoke may promote adenocarcinoma progression by activating the Notch-1 pathway thus supporting its role as hallmark of lung cancer progression and as a new target for lung cancer treatment.