Evidence map›Paper›PMID 37056808›Full record

ArticleAmerican journal of translational research2023

A pan-cancer analysis of HAVCR1 with a focus on diagnostic, prognostic and immunological roles in human cancers.

Guangyao Li, Muhammad Javed, Rubab Rasool, Mostafa A Abdel-Maksoud, Ayman S Mubarak, Christian R Studenik, J Narayanan, Sampson Agyapong Atuahene, Mohammed Aufy, Kun Cao

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Article in American journal of translational research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

10 authors at 1 institution in 2 countries.

Guangyao LiDepartment of Gastrointestinal Surgery, The Second People's Hospital of Wuhu Wuhu, Anhui, The People's Republic of China.
Muhammad JavedPrimary and Secondary Health Care Department Lahore, Pakistan.
Rubab RasoolHealth Bridge Hospital, Defense Housing Authority Lahore, Pakistan.
Mostafa A Abdel-MaksoudBotany and Microbiology Department, College of Science, King Saud University Riyadh 11451, Saudi Arabia.
Ayman S MubarakBotany and Microbiology Department, College of Science, King Saud University Riyadh 11451, Saudi Arabia.
Christian R StudenikDepartment of Pharmaceutical Sciences, Division of Pharmacology and Toxicology, University of Vienna Vienna, Austria.
J NarayananSRM College of Pharmacy SRMIST Chennai, India.
Sampson Agyapong AtuaheneDepartment of Curriculum and Pedagogy, College of Teacher Education, Zhejiang Normal University Jinhua 321004, China.
Mohammed AufyDepartment of Pharmaceutical Sciences, Division of Pharmacology and Toxicology, University of Vienna Vienna, Austria.
Kun CaoDepartment of General Surgery, The First People's Hospital of Hefei Hefei, Anhui, The People's Republic of China.
University of Health Sciences Lahore · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCancer is one of the most prominent causes of death world wide. Identification of novel cancer biomarkers woud help with cancer diagnosis and possible treatment.

methodsIn this study, we comprehensively studied the diagnostic, prognostic, and therapeutic values of the hepatitis A virus cellular receptor 1 (HAVCR1) gene across multiple cancers from a pan-cancer point of view via a detailed

resultsHAVCR1 expression was up-regulated in a variety of malignancies. The up-regulated HAVCR1 was closely related to the poor prognosis in patients with esophageal carcinoma (ESCA), lung adenocarcinoma (LUAD), and stomach adenocarcinoma (STAD). Moreover, DAVID analysis showed that HAVCR1, along with different other associated genes, was involved in numerous cancer-associated signaling pathways across ESCA, STAD, and LUAD. Furthermore, in these cancers, HAVCR1 was also found closely associated with some other parameters such as promoter methylation, tumor purity, level of CD8+ T immune cells, genomic alterations, and chemotherapeutic drugs.

conclusionHAVCR1 was overexpressed in multiple tumors. However, the up-regulated HAVCR1 is a valuable diagnostic and prognostic biomarker as well as a therapeutic target in only ESCA, STAD, and LUAD patients.

Indexed as

biomarkerHAVCR1pan-cancertherapeutic

Identifiers

PMID37056808
PMCPMC10086885
OpenAlexW4365484789

What OpenQuestion holds

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Registered trials

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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.