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Manuscript title: Activating invasion and metastasis in small cell lung cancer
  • Carl He
Carl He
Eastern Health

Corresponding Author:[email protected]

Author Profile

Abstract

Background: Small cell lung cancer (SCLC) harbours the most aggressive phenotype of all lung cancers to correlate with its bleak prognosis. The aggression of SCLC is partially attributable to its strong metastatic tendencies. The biological processes facilitating the metastasis in SCLC are still poorly understood and garnering a deeper understanding of these processes may enable the exploration of additional targets against this cancer hallmark in the treatment of SCLC. Recent findings: This narrative review will discuss the proposed molecular mechanisms by which the cancer hallmark of activating invasion and metastasis is featured in SCLC through important steps of the metastatic pathway. The review will discuss SCLC VEGF family expression and vascular mimicry as a means of vasculogenesis, and the role of tumour heterogeneity, DLL3, NFIB, selectin, and B1 integrin in enabling epithelial to mesenchymal transition and subsequent invasion, and the molecular markers expressed by SCLC to assist organ-specific homing during metastasis. The review will also discuss a recent article observing mir-1 mrna upregulation as a potential therapeutic option in targeting the metastatic activity of SCLC. Conclusion: Treatment of SCLC remains a clinical challenge due to its recalcitrant and aggressive nature. Amongst the many hallmarks used by SCLC to enable its aggressive behaviour, that of its ability to invade surrounding tissue and metastasise is particularly notable and understanding the molecular mechanisms in SCLC metastasis can identify therapeutic targets to attenuate SCLC aggression and improve mortality.
08 Mar 2024Submitted to Cancer Reports
13 Mar 2024Submission Checks Completed
13 Mar 2024Assigned to Editor
13 Mar 2024Review(s) Completed, Editorial Evaluation Pending
18 Mar 2024Reviewer(s) Assigned
10 Jul 2024Editorial Decision: Revise Major
07 Aug 20241st Revision Received
07 Aug 2024Submission Checks Completed
07 Aug 2024Assigned to Editor
07 Aug 2024Review(s) Completed, Editorial Evaluation Pending
08 Aug 2024Reviewer(s) Assigned
09 Sep 2024Editorial Decision: Accept