Small cell lung cancer: State of the art of the molecular and genetic landscape and novel perspective

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Autores organización

Autores

  • Denninghoff V
  • Russo A
  • de Miguel-Pérez D
  • Malapelle U
  • Benyounes A
  • Gittens A
  • Rolfo C

Grupos de investigación

Resumen

Small cell lung cancer (SCLC) is a highly proliferative lung cancer that is not amenable to surgery in most cases due to the high metastatic potential. Precision medicine has not yet improved patients’ survival due to the lack of actionable mutations. Intra-and intertumoral heterogeneity allow the neoplasms to adapt to various microenvironments and treatments. Further studying this heterogeneous cancer might yield the discovery of actionable mutations. First-line SCLC treatment has added immunotherapy to its armamentarium. There has been renewed interest in SCLC, and numerous clinical trials are underway with novel therapeutic approaches. Understanding the molecular and genetic landscape of this heterogeneous and lethal disease will pave the way for novel drug development. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Datos de la publicación

ISSN/ISSNe:
2072-6694, 2072-6694

Cancers  MDPI AG

Tipo:
Review
Páginas:
-
Enlace a otro recurso:
www.scopus.com

Citas Recibidas en Web of Science: 9

Citas Recibidas en Scopus: 22

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Keywords

  • CD56 antigen; chromogranin A; cyclophosphamide; DNA topoisomerase inhibitor; doxorubicin; E1A associated p300 protein; ephrin receptor A7; fibroblast growth factor receptor 1; gyrase inhibitor; homeobox protein Nkx 2.1; KMT2D protein; lurbinectedin; mammalian target of rapamycin; methyltransferase; mixed lineage leukemia protein; Myc protein; neurogenic differentiation factor; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitor; Notch receptor; phosphatidylinositol 3 kinase; phosphatidylinositol 3,4,5 trisphosphate 3 phosphatase; platinum complex; protein kinase B; protein p53; protein Ret; Slit2 protein; sonic hedgehog protein; synaptophysin; tarlatamab; transcription factor Yap1; tumor protein p73; unclassified drug; cancer genetics; cancer growth; cancer immunotherapy; cancer prognosis; cancer survival; carcinogenesis; cell cycle regulation; differentiation; enzyme activity; epigenetics; gene expression regulation; gene mutation; genetic analysis; hu

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