Pseudolaric Acid B Inhibits Proliferation, Invasion, and Angiogenesis in Esophageal Squamous Cell Carcinoma Through

Zhe Yin1, Huarong Cai1, Zhiqiang Wang1

  • 1Department of Thoracic Surgery, Chongqing University Cancer Hospital, Chongqing 400030, China.

Abstract

Insights

Pseudolaric acid B (PAB) effectively inhibits esophageal squamous cell carcinoma (ESCC) progression by targeting CD147. This natural compound shows promise for ESCC therapy by reducing cell proliferation, invasion, migration, and angiogenesis.

Area of Science:

  • Oncology
  • Pharmacology
  • Molecular Biology

Background:

  • Esophageal squamous cell carcinoma (ESCC) is a prevalent digestive system malignancy.
  • Pseudolaric acid B (PAB) exhibits known anti-microtubule, anti-angiogenesis, and antitumor properties.
  • The specific effects and mechanisms of PAB on ESCC remain largely unexplored.

Purpose of the Study:

  • To investigate the therapeutic effects of PAB on esophageal squamous cell carcinoma (ESCC).
  • To elucidate the underlying molecular mechanisms of PAB's action in ESCC.

Main Methods:

  • Conducted a series of in vitro and in vivo experiments to assess PAB's biological effects on ESCC.
  • Analyzed cell proliferation, invasion, migration, and apoptosis.
  • Investigated the role of CD147 and matrix metalloproteinases (MMPs) in PAB's mechanism of action.

Main Results:

  • PAB significantly inhibited ESCC cell proliferation, invasion, and migration while promoting apoptosis in vitro.
  • PAB suppressed tumor growth and angiogenesis in vivo.
  • PAB reduced CD147 expression, which was found to be upregulated in ESCC cells and associated with increased MMP2, 3, and 9 expression.
  • Interference with CD147 mimicked PAB's inhibitory effects on ESCC progression and angiogenesis.

Conclusions:

  • PAB exerts its anti-cancer effects on ESCC by downregulating CD147 expression, thereby inhibiting proliferation, invasion, migration, and angiogenesis.
  • PAB represents a promising therapeutic agent for ESCC, warranting further investigation for clinical application.