Evidence map›Paper›PMID 35281041›Full record

ArticleFrontiers in immunology2022

Elevated SNRPA1, as a Promising Predictor Reflecting Severe Clinical Outcome

Aimin Jiang, Jialin Meng, Wenliang Gong, Zhonghua Zhang, Xinxin Gan, Jie Wang, Zhenjie Wu, Bing Liu, Le Qu, Linhui Wang

Abstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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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.

Aimin JiangDepartment of Urology, Changhai Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.
Jialin MengDepartment of Urology, The First Affiliated Hospital of Anhui Medical University; Institute of Urology, Anhui Medical University; Anhui Province Key Laboratory of Genitourinary Diseases, Anhui Medical University, Hefei, China.
Wenliang GongDepartment of Urology, Changhai Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.
Zhonghua ZhangDepartment of Clinical Pharmacy, No. 988 Hospital of Joint Logistic Support Force, Zhengzhou, China.
Xinxin GanDepartment of Urology, Changhai Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.
Jie WangDepartment of Urology, Changhai Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.
Zhenjie WuDepartment of Urology, Changhai Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.
Bing LiuDepartment of Urology, The Third Affiliated Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.
Le QuDepartment of Urology, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Linhui WangDepartment of Urology, Changhai Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal carcinoma and is associated with poor prognosis and notorious for its immune dysfunction characteristic. SNRPA1 is a spliceosome component responsible for processing pre-mRNA into mRNA, while the biological effect of SNRPA1 in ccRCC remains elusive. The aim of this study was to decipher the effect of SNRPA1 on clinical effect and tumor immunity for ccRCC patients. Multi-databases were collected to evaluate the different expression, prognostic value, DNA methylation, tumor immune microenvironment, and drug sensitivity of SNRPA1 on ccRCC. IHC was utilized to validate the expression and prognostic value of SNRPA1 in ccRCC patients from the SMMU cohort. The knockout expression of SNRPA by sgRNA plasmid inhibited the cell proliferation, migration, and metastasis ability and significantly increased the sensitivity of sunitinib treatment. In addition, we explored the role of SNRPA1 in pan-cancer level. The results indicated that SNRPA1 was differentially expressed in most cancer types. SNRPA1 may significantly influence the prognosis of multiple cancer types, especially in ccRCC patients. Notably, SNRPA1 was significantly correlated with immune cell infiltration and immune checkpoint inhibitory genes. In addition, the aggressive and immune inhibitory effects shown in SNRPA1 overexpression and the effect of SNRPA1 on ccRCC cell line invasion, metastasis, and drug sensitivity

Indexed as

Carcinoma, Renal CellKidney NeoplasmsBiomarkers, TumorFemaleHumansMalePrognosisSunitinibTumor MicroenvironmentBiomarkers, TumorSunitinibclear cell renal cell carcinomadrug responseprognosissmall nuclear ribonucleoprotein polypeptide Atumor immunity

Identifiers

PMID35281041
PMCPMC8904888

What Socratic 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 Socratic graph.