1. Academic Validation
  2. Connexin 43 contributes to the sensitization of colorectal cancer cells to photodynamic therapy through Akt inhibition

Connexin 43 contributes to the sensitization of colorectal cancer cells to photodynamic therapy through Akt inhibition

  • Photodiagnosis Photodyn Ther. 2022 Sep;39:103040. doi: 10.1016/j.pdpdt.2022.103040.
Yijia Wang 1 Lankai Chen 2 Sizhen Lai 3 Yanfei Liu 3 Ben Yi 3 Siwei Zhu 1 Xia Hu 4 Qinghuai Zhang 5 Chunze Zhang 6
Affiliations

Affiliations

  • 1 Laboratory of Oncologic molecular medicine, Tianjin Union Medical Center, Tianjin, 300121, China.
  • 2 Nankai University School of Medicine, Nankai University, Tianjin, 300121, China.
  • 3 Tianjin University of Traditional Chinese Medicine, Tianjin, 300121, China.
  • 4 Department of Agriculture Insect, Institute of Plant Protection, Tianjin Academy of Agricultural Sciences, Tianjin, 300381, China.
  • 5 Department of Colorectal Surgery, Tianjin Union Medical Center, Tianjin 300121, China.
  • 6 Department of Colorectal Surgery, Tianjin Union Medical Center, Tianjin 300121, China. Electronic address: chunze.zhang@nankai.edu.cn.
Abstract

Background: Photodynamic therapy could be one approach to treat colorectal Cancer though resistance leads to failure of therapy. Akt activation is a cellular survival response to photodynamic therapy and is also a reason for resistance. Thus, inhibition of Akt is a strategy to decrease resistance. Akt interacts with connexin 43, another protein involved in photodynamic therapy resistance. Connexin 43 is widely expressed in different human tissues and has a complex role in tumor development. However, the mechanism of inhibition of Akt by connexin 43 that sensitizes colorectal Cancer cells to photodynamic therapy needs further investigation.

Methods: In this study, two colorectal Cancer cells with low phosphorylated connexin 43 level were used to explore this mechanism. LY294002 was used as an Akt Inhibitor, and connexin 43-pCMV3 was transfected into cells to increase connexin 43 expression.

Results: Akt and connexin 43 inhibit each Other in both colorectal Cancer cell lines. In vitro and in vivo experiments showed that LY294002 and connexin 43 transfection sensitized cells to hematoporphyrin-Photodynamic therapy. LY294002 increased the sensitivity of cells to photodynamic therapy with a pronounced effect in cells with high expression levels of connexin 43.

Conclusions: Connexin 43 should be considered an important factor in increasing the phototoxicity of photodynamic therapy in colorectal Cancer through Akt inhibition.

Keywords

Akt activation; Connexin 43; Photodynamic Therapy; Resistance.

Figures
Products