RNA splicing alterations in lung cancer pathogenesis and therapy.

Cancer Pathog Ther

Department of Cellular and Genetic Medicine, Shanghai Key Laboratory of Medical Imaging Computing and Computer Assisted Intervention, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.

Published: October 2023

AI Article Synopsis

  • - RNA splicing changes are common in lung cancer and significantly impact its development and treatment options, making this a vital area of research.
  • - Large-scale studies have identified various genetic and transcriptional changes in lung cancer, aiding in the creation of new diagnostic tools and therapies over the years.
  • - The article discusses how targeting splicing alterations, along with existing treatments, could provide new strategies to manage lung cancer, highlighting recent advancements in understanding splicing-related mechanisms.

Article Abstract

RNA splicing alterations are widespread and play critical roles in cancer pathogenesis and therapy. Lung cancer is highly heterogeneous and causes the most cancer-related deaths worldwide. Large-scale multi-omics studies have not only characterized the mutational landscapes but also discovered a plethora of transcriptional and post-transcriptional changes in lung cancer. Such resources have greatly facilitated the development of new diagnostic markers and therapeutic options over the past two decades. Intriguingly, altered RNA splicing has emerged as an important molecular feature and therapeutic target of lung cancer. In this review, we provide a brief overview of splicing dysregulation in lung cancer and summarize the recent progress on key splicing events and splicing factors that contribute to lung cancer pathogenesis. Moreover, we describe the general strategies targeting splicing alterations in lung cancer and highlight the potential of combining splicing modulation with currently approved therapies to combat this deadly disease. This review provides new mechanistic and therapeutic insights into splicing dysregulation in cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10846331PMC
http://dx.doi.org/10.1016/j.cpt.2023.04.004DOI Listing

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