Evidence map›Paper›PMID 36419887›Full record

ArticleFrontiers in oncology2022

The expression and prognostic value of transporter 1, ATP binding cassette subfamily B member in clear cell renal cell cancer with experimental validation.

Zhen-Da Wang, Xi Tian, Yue Wang, Jun-Jie Wang, Shi-Qi Ye, Yong-Qiang Huang, Yuan-Yuan Qu, Kun Chang, Guo-Hai Shi, Ding-Wei Ye and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. 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
1.6field-weighted citation impact, top 15% 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, 16 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

11 authors at 2 institutions in 1 country.

Zhen-Da WangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xi TianDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yue WangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jun-Jie WangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Shi-Qi YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yong-Qiang HuangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yuan-Yuan QuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Kun ChangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Guo-Hai ShiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ding-Wei YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Cheng-Yuan GuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Shanghai Medical College of Fudan University · CNFudan University Shanghai Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transporter associated with antigen processing 1(TAP1) serves as a protein to transport antigenic peptides from the surface of the endoplasmic reticulum to the lumen of the endoplasmic reticulum when the antigens are presented by major histocompatibility complex type I (MHC-I), which has been identified to play a critical role in antigen presentation in innate immunity. In tumors, the role of TAP1 seems to remain controversial. On the one hand, given the role of TAP1 in antigen presentation, it is indicated that high TAP1 expression corresponds to the emergence of more neoantigens epitopes that facilitate the recognition for phagocytes, T cells and other cells. On the other hand, the genetic ablation of transporter associated with antigen processing (TAP) results in the presentation of new class I-restricted epitopes encoded in house-keeping products. Opposite result has been revealed by studies in other tumors suggest, which implies a more complex function of TAP1. Therefore, it's significant to clarify the role of TAP1 in clear cell renal cell carcinoma (ccRCC). In this study, we found the elevated expression levels in mRNA and protein of TAP1 in ccRCC tissues, which indicated a relatively worse prognosis. Transwell assay and Scratch assay

Indexed as

clear cell renal cell carcinomaprognosisTAP1therapeutic biomarkertumor immune microenvironment

Identifiers

PMID36419887
PMCPMC9676953
OpenAlexW4308448244

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.