4.6 Article

Increased expression of METTL3 in pancreatic cancer tissues associates with poor survival of the patients

期刊

WORLD JOURNAL OF SURGICAL ONCOLOGY
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12957-022-02743-7

关键词

METTL3; Pancreatic cancer; Immunohistochemistry; Prognosis

资金

  1. National Natural Science Foundation of China [82172689, 81902386]
  2. China Postdoctoral Science Foundation [2021M700543, 2021M700547]
  3. High-Level Talents Project of Jiangsu Commission of Health [LGY2020034]
  4. Changzhou International Cooperation Project [CZ20210035]
  5. Applied Basic Research Foundation of Changzhou [CJ20190094, CJ20210089]
  6. Changzhou High-Level Medical Talents Training Project [2016CZBJ001]
  7. Major Program of Science and Technology Project of Changzhou Health Commission [ZD202102]
  8. Young Talent Development Plan of Changzhou Health Commission (2020-233) [CZQM2020044]

向作者/读者索取更多资源

This study found that METTL3 expression is increased in pancreatic cancer tissues and is associated with the progression and prognosis of the disease. Additionally, METTL3 expression is related to tumor-infiltrating immune cells and m(6)A modification and metabolism in pancreatic cancer tissues.
Background Methyltransferase-like 3 (METTL3) expression could be found in various normal and cancerous tissues. As of now, the clinical significance of METTL3 expression in human pancreatic cancer (PC) tissues still remains to be understood. Our present study aims to investigate the prognostic value and clinical implications of METTL3 expression in PC tissues. Methods The TCGA, GTEx, and GEO public databases were used to study the mRNA expression level of the m(6)A family members and its relationship among PC tissues and normal pancreatic tissue. The immunohistochemistry was used to analyze the difference of METTL3 expression between cancer tissues and adjacent normal tissues. The prognostic value was evaluated by using the Log-rank survival analysis and Cox model analysis. PAAD samples from TCGA and GEO databases were used to perform the immune infiltration analysis and gene set enrichment analysis based on the genes that were highly correlated with METTL3. Results Based on the analysis of TCGA, GTEx, and GEO public database, we found that the m(6)A family members showed a higher correlation in PC tissues compared to normal pancreatic tissues, and the mRNA expression level of the m(6)A family members showed a significant difference between PC tissues and adjacent normal tissues. Moreover, scRNA-seq data indicated that METTL3 showed a higher expression level in malignant epithelial cells. Our immunohistochemistry results also confirmed that the intensity of METTL3 immunostaining in PC tissues was significantly higher than that in adjacent normal tissues (P = 0.015). The overall survival (OS) of PC patients with high expression of METTL3 protein were significantly poorer than those with low expression of METTL3 protein (HR = 1.788, 95% CI 1.071-2.984, P = 0.026). Further analysis of PC data from the database showed that METTL3 expression was associated with a variety of tumor-infiltrating immune cells and was involved in m(6)A modification and metabolism in PC tissues. Conclusion Increased METTL3 expression at the protein level could be found in PC tissues, suggesting that the METTL3 expression was involved in the progression of PC and could serve as an important marker for prognostic prediction of this malignancy.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据