Anlotinib suppressed tumor cell proliferation and migration in hypopharyngeal carcinoma

Hao Song1, Qing Song2, Xiangkun Zhao1

  • 1The Second Medical College, Binzhou Medical University, Yantai, China; Department of Otorhinolaryngology Head and Neck Surgery, Yantai Yuhuangding Hospital, Qingdao University, Yantai, China; Yantai Key Laboratory of Otorhinolaryngologic Diseases, Yantai, China; Shandong Provincial Clinical Research Center for Otorhinolaryngologic Diseases, Yantai, China.

Abstract

Insights

Anlotinib effectively inhibits hypopharyngeal cancer cell growth and migration in vitro. This multitarget inhibitor promotes apoptosis and blocks cell cycle progression, offering a potential new treatment for hypopharyngeal cancer.

Area of Science:

  • Oncology
  • Pharmacology
  • Molecular Biology

Background:

  • Hypopharyngeal cancer presents a significant therapeutic challenge.
  • Novel therapeutic strategies are urgently needed to improve patient outcomes.

Purpose of the Study:

  • To investigate the in-vitro anti-cancer effects of anlotinib on hypopharyngeal cancer cells.
  • To elucidate the underlying molecular mechanisms of anlotinib's action.
  • To evaluate anlotinib as a potential therapeutic agent for hypopharyngeal cancer.

Main Methods:

  • Hypopharyngeal cancer Fadu cells were treated with varying concentrations of anlotinib.
  • Cell proliferation was assessed using CCK-8 and colony-forming assays.
  • Cell migration and invasion were evaluated via wound-healing and Transwell assays.
  • Cell cycle distribution and apoptosis were analyzed by flow cytometry.
  • Gene expression changes were measured using RT-qPCR and Western blot.

Main Results:

  • Anlotinib significantly inhibited Fadu cell proliferation and colony formation.
  • Anlotinib demonstrated potent inhibition of cell migration and invasion.
  • Flow cytometry revealed that anlotinib induced G2/M cell cycle arrest and promoted apoptosis.
  • Anlotinib treatment led to a decrease in HIF-1α expression.

Conclusions:

  • Anlotinib exhibits significant anti-proliferative, anti-migratory, and anti-invasive effects on hypopharyngeal cancer cells in-vitro.
  • The anti-tumor activity of anlotinib is mediated by cell cycle arrest at G2/M phase and induction of apoptosis.
  • Reduced HIF-1α expression may contribute to anlotinib's anti-cancer effects.
  • Anlotinib represents a promising therapeutic candidate for hypopharyngeal cancer treatment.