HepG2 cells recovered from apoptosis show altered drug responses and invasiveness

Shan Shan Wang, Xin Xie, Chung Sing Timothy Wong, Pui Ying Choi, Ming Chiu Fung

Research output: Contribution to journalArticlepeer-review

Abstract

BACKGROUND: Cancer relapse, associated with increased drug resistance and rate of metastasis, often follows completion of chemotherapy but the cancer escape mechanisms are still incompletely understood. Percutaneous ethanol injection (PEI) has been used for treating hepatocellular carcinoma (HCC) for decades, while the recurrence after PEI treatment remains a major limitation. Recent evidence mounted that cancer cells could survive from chemical induced apoptosis, suggesting a potential route through which cancer relapse may occur. This study focuses on the consequence of HepG2 recovery from ethanol-induced apoptotic event. METHODS: The model of HepG2 recovery from ethanolinduced apoptotic event was established by live cell imaging, BrdU assay and Western blotting. MTT assay, wound healing assay and invasion assay were used to investigate the behavior of HepG2 after recovery. RESULTS: HepG2 cells could recover from ethanol-induced apoptosis. These cells changed their behaviors such as drug resistance, mobility and invasiveness. On average, the recovered HepG2 cell clones were found to be 46% more resistant to ethanol and 84% higher in mobility. The recovered clones became 58.2% more sensitive to 5-fluorouracil. CONCLUSIONS: HepG2 cells can recover from ethanolinduced apoptotic event. These cells became more resistant to ethanol and more invasive. Although the recovered cell clones were more resistant to ethanol, they became more sensitive to 5-fluorouracil treatment.

Original languageEnglish (US)
Pages (from-to)293-300
Number of pages8
JournalHepatobiliary and Pancreatic Diseases International
Volume13
Issue number3
DOIs
StatePublished - 2014

Keywords

  • 5-fluorouracil
  • Apoptosis
  • Cancer recurrence
  • Liver cancer
  • Percutaneous ethanol injection
  • Recovery

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

Fingerprint Dive into the research topics of 'HepG2 cells recovered from apoptosis show altered drug responses and invasiveness'. Together they form a unique fingerprint.

Cite this