4.6 Article

Epigenetic landscape of small cell lung cancer: small image of a giant recalcitrant disease

期刊

SEMINARS IN CANCER BIOLOGY
卷 83, 期 -, 页码 57-76

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2020.11.006

关键词

Epigenetic modifications; Histone acetylation; DNA methylation; Small cell lung cancer; Neuroendocrine carcinoma

类别

资金

  1. National Institutes of Health (NIH) [R01CA218545]
  2. VA [I01 BX004676]
  3. National Cancer Institute of the NIH [R01CA218545, P30CA033572, 1U54CA209978-01A1, R01CA247471]
  4. NIH [R01CA247471, R01CA195586]

向作者/读者索取更多资源

SCLC is a subtype of lung cancer with high mortality, where epigenetic modifications play a crucial role in tumorigenesis, progression, and drug resistance. Understanding SCLC epigenetics is important for prognostication, treatment stratification, and the development of new therapies.
Small cell lung cancer (SCLC) is a particular subtype of lung cancer with high mortality. Recent advances in understanding SCLC genomics and breakthroughs of immunotherapy have substantially expanded existing knowledge and treatment modalities. However, challenges associated with SCLC remain enigmatic and elusive. Most of the conventional drug discovery approaches targeting altered signaling pathways in SCLC end up in the `grave-yard of drug discovery', which mandates exploring novel approaches beyond inhibiting cell signaling pathways. Epigenetic modifications have long been documented as the key contributors to the tumorigenesis of almost all types of cancer, including SCLC. The last decade witnessed an exponential increase in our understanding of epigenetic modifications for SCLC. The present review highlights the central role of epigenetic regulations in acquiring neoplastic phenotype, metastasis, aggressiveness, resistance to chemotherapy, and immunotherapeutic approaches of SCLC. Different types of epigenetic modifications (DNA/histone methylation or acetylation) that can serve as predictive biomarkers for prognostication, treatment stratification, neuroendocrine lineage determination, and development of potential SCLC therapies are also discussed. We also review the utility of epigenetic targets/epidrugs in combination with first-line chemotherapy and immunotherapy that are currently under investigation in preclinical and clinical studies. Altogether, the information presents the inclusive landscape of SCLC epigenetics and epidrugs that will help to improve SCLC outcomes.

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