mRNA and protein of p33ING1 in normal and cancer tissues

Shuang Zhao1, Hua-Chuan Zheng1

  • 1Department of Experimental Oncology, Shengjing Hospital of China Medical University, Shenyang 110004, China.

Abstract

Insights

Inhibitor of growth protein 1 (ING1) expression, particularly ING1b mRNA, is elevated in many cancers and correlates with better survival in gastric patients. The p33ING1 protein shows varied localization, suggesting roles in tissue repair and epithelial carcinogenesis.

Area of Science:

  • Molecular oncology
  • Cancer biology
  • Tumor suppressor genes

Background:

  • Inhibitor of growth protein 1 (ING1) acts as a tumor suppressor.
  • ING1 down-regulation is linked to cancer progression and aggressiveness.
  • ING1 interacts with H3K4me3 and p53, influencing cellular processes.

Purpose of the Study:

  • To investigate the relationship between ING1b mRNA expression and patient survival rates.
  • To determine the expression profiles and subcellular localization of the p33ING1 protein in various human and mouse tissues, including cancerous ones.

Main Methods:

  • Analysis of ING1b mRNA expression datasets correlated with survival.
  • Immunohistochemistry to assess p33ING1 protein expression in tissue microarrays.
  • Examination of normal and cancerous tissues from mice and humans.

Main Results:

  • ING1b mRNA was highly expressed in colorectal, lung, and breast cancers, correlating positively with survival in gastric cancer.
  • p33ING1 protein localization was predominantly nuclear in mouse tissues but varied (nuclear, cytoplasmic, nucleocytoplasmic) in human tissues.
  • p33ING1 was detected in various normal human tissues; its expression varied in cancer, with strong detection in stomach, trachea, skin, cervix, and breast. Overall positive rate was 41.0% in tested cancers.

Conclusions:

  • p33ING1 may play a role in organ/tissue repair and regeneration.
  • The protein is potentially involved in the carcinogenesis of highly proliferative epithelia.
  • Expression patterns suggest context-dependent functions of p33ING1 in cancer.