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Updated: Jun 2, 2026

Multiomics Analysis of TMEM200A as a Pan-Cancer Biomarker
Published on: September 15, 2023
The expression of stat91, ras-independent signal transducer and activator, in human gastric carcinomas
K Kitahara1, W Yasui, H Kuniyasu
1HIROSHIMA UNIV,SCH MED,DEPT PATHOL 1,MINAMI KU,HIROSHIMA 734,JAPAN. SAGA MED SCH,DEPT SURG,SAGA 849,JAPAN.
Abstract:
Upon binding of interferon (IFN) and epidermal growth factor (EGF) to their cell surface receptors, tyrosine phosphorylation of latent cytoplasmic Stat91 (Ras-independent signal transducer and activator of transcription, Stat1 alpha) protein is promptly induced and translocate from the cytoplasm to the nucleus to transduce the signal. The expression of mRNA for Stat91 was examined in 8 gastric carcinoma cell lines and 21 gastric carcinoma tissues as well as corresponding normal mucosa. Of the 8 gastric carcinoma cell lines, all expressed a 4.7 kb Stat91 mRNA and a 91 kD protein at various levels. In gastric carcinoma cell lines, the levels of Stat91 mRNA expression were compatible with those of Stat91 protein expression. In surgical cases, all the gastric carcinoma tissues and their adjacent non-neoplastic mucosa expressed Stat91 mRNA and protein. Interestingly, 14 (66%) out of 21 tumors expressed Stat91 mRNA at higher levels than their corresponding normal mucosas. Moreover, 6 (75%) of 8 tumor tissues expressed higher levels of Stat91 protein as compared with those of the corresponding normal gastric mucosa. No significant correlation was detected between the expression of Stat91 and clinicopathological feature of gastric carcinoma. These results suggest that the majority of gastric cancer in vivo harbour overexpression of Stat91 as a signal transducer in response to various cytokines or growth factors which may be implicated in the growth of gastric cancer.
Insights
Signal transducer and activator of transcription (Stat91) protein is overexpressed in most gastric cancers. This overexpression may contribute to gastric cancer growth by mediating signals from growth factors and cytokines.
Area of Science:
- Molecular biology
- Oncology
- Cell signaling
Background:
- Interferon (IFN) and epidermal growth factor (EGF) activate cytoplasmic Stat91 protein via tyrosine phosphorylation.
- Activated Stat91 translocates to the nucleus to regulate gene expression.
Purpose of the Study:
- To investigate Stat91 mRNA and protein expression in gastric carcinoma cell lines and tissues.
- To determine the correlation between Stat91 expression and gastric cancer development.
Main Methods:
- Analysis of Stat91 mRNA and protein levels in 8 gastric carcinoma cell lines.
- Examination of Stat91 mRNA and protein expression in 21 gastric carcinoma tissues and adjacent normal mucosa.
Main Results:
- All 8 gastric carcinoma cell lines expressed Stat91 mRNA and protein.
- 14 out of 21 (66%) gastric tumors showed higher Stat91 mRNA levels than normal mucosa.
- 6 out of 8 (75%) tumor tissues exhibited higher Stat91 protein levels compared to normal gastric mucosa.
Conclusions:
- The majority of gastric cancers exhibit Stat91 overexpression.
- Stat91 may play a role in gastric cancer growth by transducing signals from cytokines and growth factors.
- No significant correlation was found between Stat91 expression and clinicopathological features of gastric carcinoma.
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