Evidence map›Paper›PMID 36779496›Full record

ArticleCancer medicine2023

Molecular genetic and clinical characteristic analysis of primary signet ring cell carcinoma of urinary bladder identified by a novel OR2L5 mutation.

Mohammed Alradhi, Shuang Wen, Mohammed Safi, Abdullah Al-Danakh, Honglong Wang, Abdullah Shopit, Min Sun, Bo Fan, Xiancheng Li

Open access · goldAbstract readCase Reports
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 8 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

9 authors at 4 institutions in 1 country.

Mohammed AlradhiDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, China.ORCID 0000-0001-8003-227X
Shuang WenDepartment of Pathology, Dalian Friendship Hospital, Dalian, China.
Mohammed SafiDepartment of Respiratory Diseases, Shandong Second Provincial General Hospital Shandong University, Shandong, China.ORCID 0000-0001-7928-2343
Abdullah Al-DanakhDepartment of Urology, First Affiliated Hospital of Dalian Medical University, Dalian, China.ORCID 0000-0003-1612-4190
Honglong WangDepartment of Pathology, Dalian Friendship Hospital, Dalian, China.
Abdullah ShopitDepartment of Pharmacology, Dalian Medical University, Dalian, China.
Min SunDepartment of General Surgery, Taihe Hospital, Hubei University of Medicine, Hubei, China.
Bo FanDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, China.ORCID 0000-0001-6598-3237
Xiancheng LiDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, China.ORCID 0000-0002-8301-2589
Dalian Medical University · CNYili Friendship Hospital · CNHubei University of Medicine · CNSecond Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To get a better understanding of the genetic basis of primary signet ring cell carcinoma (SRCC) of the bladder, which is highly rare and not yet explored. First, by using immunohistochemistry to find histological pathological characteristics. Second, a massively parallel whole-exome sequencing (WES) was performed on a 58-year-old male patient who had painless macroscopic hematuria and was pathologically diagnosed with primary SRCC of the bladder, followed by comparing with genes of ordinary urothelial cancer (UC) from TCGA. Furthermore, a population-based analysis using the SEER database was performed to investigate the prognosis (SRCC vs. UC). We identified 63 copy number variations (CNVs) with gain counts and 181 CNVs with loss counts. Totally 4515 mutations were discovered in C > T with a success rate of greater than 89%. The most frequently mutated pathway was RTK-RAS which has 85 genes involved in carcinogenic signaling. Final screening on predisposing genes is performed after filtering based on ACMG. Moreover, several driver genes, including NBN, KCTD18, SPATA13, ANKRD36, OR2L5, MALRD1, and LSMEM1, were detected. Sanger sequencing of germline DNA revealed the presence of a mutant base A/G of OR2L5 in the sequence, which was discovered for the first time in primary SRCC of the bladder. Furthermore, the immunohistochemical profile showed that primary SRCC of the bladder were positive for CK7, CK20, GATA-3, and expression of CK(AE1/AE2), EMA, and Ki67. In the SEER-based study, the patients with primary SRCC of the bladder got a worse prognosis compared to those with UC with median months overall survival (OS) 14 vs. 41, respectively, P = 0001, even after adjusting the variables in the Cox regression model, the SRCC of the bladder showed worse survival HR = 1.119, 95% CI = (1.081-1.328), P = 0.0001. These results imply that suppression of potential driver mutations may be a viable adjuvant treatment approach for primary SRCC in the bladder in place of standard chemotherapy, a possibility that warrants further clinical investigation.

Indexed as

Carcinoma, Signet Ring CellCarcinoma, Transitional CellUrinary Bladder NeoplasmsDNA Copy Number VariationsHumansMaleMiddle AgedMolecular BiologyMutationReceptors, OdorantUrinary BladderOR2L5 protein, humanReceptors, OdorantimmunohistochemistryOR2L5primary signet ring cell carcinomaurinary bladderwhole-exome sequencing

Identifiers

PMID36779496
PMCPMC9972163
OpenAlexW4292790947

What Socratic 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 Socratic graph.