| Literature DB >> 33718595 |
Anna Schwendenwein1, Zsolt Megyesfalvi1,2,3, Nandor Barany1,3,4, Zsuzsanna Valko1,3, Edina Bugyik3, Christian Lang1, Bence Ferencz2,3, Sandor Paku4, Andras Lantos3, Janos Fillinger2,3, Melinda Rezeli5, Gyorgy Marko-Varga5, Krisztina Bogos3, Gabriella Galffy6, Ferenc Renyi-Vamos2,3, Mir Alireza Hoda1, Walter Klepetko1, Konrad Hoetzenecker1, Viktoria Laszlo1,2,3, Balazs Dome1,2,3.
Abstract
Small cell lung cancer (SCLC; accounting for approximately 13%-15% of all lung cancers) is an exceptionally lethal malignancy characterized by rapid doubling time and high propensity to metastasize. In contrast to the increasingly personalized therapies in other types of lung cancer, SCLC is still regarded as a homogeneous disease and the prognosis of SCLC patients remains poor. Recently, however, substantial progress has been made in our understanding of SCLC biology. Advances in genomics and development of new preclinical models have facilitated insights into the intratumoral heterogeneity and specific genetic alterations of this disease. This worldwide resurgence of studies on SCLC has ultimately led to the development of novel subtype-specific classifications primarily based on the neuroendocrine features and distinct molecular profiles of SCLC. Importantly, these biologically distinct subtypes might define unique therapeutic vulnerabilities. Herein, we summarize the current knowledge on the molecular profiles of SCLC subtypes with a focus on their potential clinical implications.Entities:
Keywords: heterogeneity; molecular profile; neuroendocrine; small cell lung cancer
Year: 2021 PMID: 33718595 PMCID: PMC7917449 DOI: 10.1016/j.omto.2021.02.004
Source DB: PubMed Journal: Mol Ther Oncolytics ISSN: 2372-7705 Impact factor: 7.200