Evidence map›Paper›PMID 33747255›Full record

ArticleDisease markers2021

Identification of Prognostic and Therapeutic Biomarkers among FAM83 Family Members for Pancreatic Ductal Adenocarcinoma.

Zuyi Ma, Zixuan Zhou, Hongkai Zhuang, Zhenchong Li, Zuguang Ma, Bowen Huang, Chunsheng Liu, Yuanfeng Gong, Yiping Zou, Zehao Zheng and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 20% of its field
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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
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

13 authors at 4 institutions in 1 country.

Zuyi Ma *Department of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.ORCID https://orcid.org/0000-0002-8517-7600
Zixuan Zhou *Department of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.
Hongkai Zhuang *Department of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.ORCID https://orcid.org/0000-0002-4106-8736
Zhenchong LiDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.
Zuguang MaSanshui Disease Prevention Cure Station, Foshan 528100, China.
Bowen HuangDepartment of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Chunsheng LiuDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.
Yuanfeng GongDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.
Yiping ZouDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.ORCID https://orcid.org/0000-0003-2880-2147
Zehao ZhengDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.
Shanzhou HuangDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.ORCID https://orcid.org/0000-0002-7575-5841
Chuanzhao ZhangDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.ORCID https://orcid.org/0000-0001-6553-4458
Baohua HouDepartment of General Surgery, Guangdong Provincial People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510080, China.ORCID https://orcid.org/0000-0002-4239-1367
Guangdong Provincial People's Hospital · CNShantou University · CNChinese Center For Disease Control and Prevention · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Family with sequence similarity 83 (FAM83) members were shown recently to have oncogenic effect in a variety of cancer types, but the biological roles and prognostic value of FAM83 family in pancreatic ductal adenocarcinoma remain unknown. In the current study, the clinical significance and molecular function of the FAM83 family were assessed by multiple bioinformatics analysis. Besides, potential associations between differentially expressed genes (DEGs) of FAM83 family and antitumor immunity were evaluated using TIMER and TISIDB analyses. As the results show, FAM83A, FAM83D, FAM83E, and FAM83H were significantly upregulated in PDAC and were identified as DEGs. Higher expression of FAM83A, FAM83B, FAM83D, FAM83E, and FAM83H were associated with advanced tumor stage or worse patient prognosis. Importantly, the overexpression of DEGs was found to be significantly correlated with activated KRAS and loss of SMAD4, which are important drivers for PDAC. Further, FAM83A, FAM83D, and FAM83H were associated with CD8

Indexed as

Biomarkers, TumorCarcinoma, Pancreatic DuctalCell Cycle ProteinsCell MovementHumansMicrotubule-Associated ProteinsNeoplasm InvasivenessNeoplasm ProteinsPancreatic NeoplasmsProteinsProto-Oncogene Proteins p21(ras)Smad4 ProteinT-LymphocytesUp-RegulationBiomarkers, TumorCell Cycle ProteinsFAM83A protein, humanFAM83D protein, humanFAM83H protein, humanKRAS protein, humanMicrotubule-Associated ProteinsNeoplasm ProteinsProteinsProto-Oncogene Proteins p21(ras)Smad4 ProteinSMAD4 protein, human

Identifiers

PMID33747255
PMCPMC7943308
OpenAlexW3134625253

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.