癌症研究
医学
表观遗传学
生物标志物
组蛋白
染色质
肺癌
生物
肿瘤科
DNA
生物化学
遗传学
基因
作者
Daniela Scattolin,Alessandro Dal Maso,Alessandra Ferro,S. Frega,Laura Bonanno,Valentina Guarneri,Giulia Pasello
标识
DOI:10.1016/j.ctrv.2024.102768
摘要
Highlights•SCLC is a cancer with poor prognosis and lacks from predictive biomarkers.•SLFN11 is an emerging biomarker in SCLC with a prognostic role in different cancers.•SLFN11 blocks the replication fork under DNA stress and prevents tumor growth.•When downregulated, SLFN11 has negative predictive role to many anticancer drugs.•The silencing of SLFN11 could be overcome with different promising strategies.Graphical abstractAbstractSmall cell lung cancer (SCLC) is characterized by a dismal prognosis. Many efforts have been made so far for identifying novel biomarkers for a personalized treatment for SCLC patients. Schlafen 11 (SLFN11) is a protein differently expressed in many cancers and recently emerged as a new potential biomarker. Lower expression of SLFN11 correlates with a worse prognosis in SCLC and other tumors. SLFN11 has a role in tumorigenesis, inducing replication arrest in the presence of DNA damage through the block of the replication fork. SLFN11 interacts also with chromatin accessibility, proteotoxic stress and mammalian target of rapamycin signalling pathway. The expression of SLFN11 is regulated by epigenetic mechanisms, including promoter methylation, histone deacetylation, and the histone methylation. The downregulation of SLFN11 correlates with a worse response to topoisomerase I and II inhibitors, alkylating agents, and poly ADP-ribose polymerase inhibitors in different cancer types. Some studies exploring strategies for overcoming drug resistance in tumors with low levels of SLFN11 showed promising results. One of these strategies includes the interaction with the Ataxia Telangiectasia and Rad3-related pathway, constitutively activated and leading to cell survival and tumor growth in the presence of low levels of SLFN11. Furthermore, the expression of SLFN11 is dynamic through time and different anticancer therapy and liquid biopsy seems to be an attractive tool for catching SLFN11 different expressions. Despite this, further investigations exploring SLFN11 as a predictive biomarker, its longitudinal changes, and new strategies to overcome drug resistances are needed.
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