| Literature DB >> 33922215 |
Vanesa Gregorc1, Chiara Lazzari1, Mario Mandalá2,3, Stefania Ippati1, Alessandra Bulotta1, Maria Giulia Cangi4, Abdelrahman Khater5, Maria Grazia Viganò1, Aurora Mirabile1, Lorenza Pecciarini4, Francesca Rita Ogliari1, Gianluigi Arrigoni4, Greta Grassini4, Giulia Veronesi6, Claudio Doglioni4.
Abstract
Tailored therapies based on the identification of molecular targets currently represent a well-established therapeutic scenario in the treatment of non-small cell lung cancer (NSCLC) patients. However, while aiming to improve patients' response to therapy, development of resistance is frequently observed in daily clinical practice. Intratumoral heterogeneity is a frequent event in NSCLC, responsible for several critical issues in patients' diagnosis and treatment. Advances in single-cell sequencing technologies have allowed in-depth profiling of tumors and attributed intratumoral heterogeneity to genetic, epigenetic, and protein modification driven diversities within cancer cell populations. This review highlights current research on the biological role of tumor heterogeneity and its impact on the development of acquired resistance in NSCLC patients.Entities:
Keywords: NSCLC; genomic instability; non-small cell lung cancer; targeted agents; tumor heterogeneity
Year: 2021 PMID: 33922215 DOI: 10.3390/cancers13092023
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639