Evidence map›Paper›PMID 37313463›Full record

ArticleFrontiers in oncology2023

Clinical and genetic characteristics in pancreatic cancer from Chinese patients revealed by whole exome sequencing.

Yonggang He, Wen Huang, Yichen Tang, Yuming Li, Xuehui Peng, Jing Li, Jing Wu, Nan You, Ling Li, Chuang Liu and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Fusion genes in pancreatic tumors.Trends in cancer · 2024
    Review
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yonggang HeDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Wen HuangDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Yichen TangDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Yuming LiDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Xuehui PengDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Jing LiDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Jing WuDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Nan YouDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Ling LiDepartment of Medicine, Yinfeng Gene Technology Co Ltd, Jinan, China.
Chuang LiuDepartment of Medicine, Yinfeng Gene Technology Co Ltd, Jinan, China.
Lu ZhengDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Xiaobing HuangDepartment of Hepatobiliary, The Second Affiliated Hospital of Army Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pancreatic ductal adenocarcinoma (PDAC) is one of the most fatal malignancies worldwide, mostly as a result of the absence of early detection and specific treatment solutions. Consequently, identifying mutational profiles and molecular biomarkers is essential for increasing the viability of precision therapy for pancreatic cancer. Methods: We collected blood and tumor tissue samples from 47 Chinese pancreatic cancer patients and used whole-exome sequencing (WES) to evaluate the genetic landscape. Results: Our results showed the most frequently somatic alteration genes were KRAS (74.5%), TP53(51.1%), SMAD4 (17%), ARID1A (12.8%), CDKN2A (12.8%), TENM4 (10.6%), TTN (8.5%), RNF43(8.5%), FLG (8.5%) and GAS6 (6.4%) in Chinese PDAC patients. We also found that three deleterious germline mutations (ATM c.4852C>T/p. R1618*, WRN c.1105C>T/p. R369*, PALB2 c.2760dupA/p. Q921Tfs*7) and two novel fusions (BRCA1-RPRML, MIR943 (intergenic)-FGFR3). When compared to the Cancer Genome Atlas (TCGA) database, there is a greater mutation frequency of TENM4 (10.6% vs. 1.6%, Conclusions: We exhibited real-world genetic traits and new alterations in Chinese individuals with cancer of the pancreas, which might have interesting implications for future individualized therapy and medication development.

Indexed as

gene mutationKRASpancreatic ductal adenocarcinoma (PDAC)PD-L1TMBwhole-exome sequencing

Identifiers

PMID37313463
PMCPMC10258306

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.