Evidence map›Paper›PMID 40854626›Full record

ArticleJournal, genetic engineering & biotechnology2025

Gender-specific insights into TTN mutation: potential biomarker for female risk in kidney renal clear cell carcinoma.

Ayan Saha, Senzuti Sharmin, Tazin Ahmed, Sadia Tabassum, Ayan Roy, Pallab Kar, Paromita Biswas, Jannatul Ferdoush

Abstract read
In one paragraph

Article in Journal, genetic engineering & biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Ayan SahaDepartment of Biological Sciences, Asian University for Women, Chittagong 4000, Bangladesh. Electronic address: ayan.saha.bd@gmail.com.
Senzuti SharminDepartment of Biochemistry and Microbiology, North South University, Dhaka 1229, Bangladesh; Science and Math Program, Asian University for Women, Chattogram 4000, Bangladesh.
Tazin AhmedDepartment of Applied Science, Wrexham Glyndwr University, Wrexham LL11 2AW, United Kingdom; Department of Genetic Engineering and Biotechnology, East West University, Dhaka 1212, Bangladesh.
Sadia TabassumDepartment of Applied Science, Wrexham Glyndwr University, Wrexham LL11 2AW, United Kingdom; Department of Genetic Engineering and Biotechnology, East West University, Dhaka 1212, Bangladesh.
Ayan RoyDepartment of Biological Sciences, Asian University for Women, Chittagong 4000, Bangladesh.
Pallab KarAfrican Medicinal Flora and Fauna Research Niche, Walter Sisulu University, Mthatha 5117, South Africa.
Paromita BiswasDepartment of Genetic Engineering and Biotechnology, East West University, Dhaka 1212, Bangladesh.
Jannatul FerdoushDepartment of Biology, Geology and Environmental Science, University of Tennessee at Chattanooga, 615 McCallie Ave, Chattanooga, TN 37403, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kidney Renal Clear Cell Carcinoma (KIRC) is a leading cause of cancer death worldwide, but its early detection remains hindered by a lack of genetic markers. Our study aims to find prospective biomarkers that could serve as prognostic indicators and help in the identification of efficient drug candidates for KIRC treatment. Importantly, this study identifies the hub genes that play a crucial role in KIRC and their impact on male and female patients. The cBioPortal was used to identify frequently mutated genes across seven KIRC studies. Additionally, GSE168845 was employed to identify the differentially expressed genes. The analysis revealed that the titin (TTN) gene was mutated and upregulated in KIRC. Subsequently, differential genes of wild-type TTN versus mutant TTN were identified using TNMplot. The NetworkAnalyst tool was used to conduct KEGG analysis and PPI analysis on these genes. Furthermore, the Kaplan-Meier Plotter was utilized to perform overall survival analysis. Our findings indicated that the TTN gene leads to poorer prognosis in women than in men. We also discovered that the female-specific prolactin signaling pathway plays a significant role in the progression of KIRC. Moreover, our study suggested that the GDF15 gene, involved in the prolactin signaling pathway, has a worse prognosis for KIRC in women than in men. Additionally, mRNA expression analysis showed a negative correlation between GDF15 and MAPK14 in KIRC. Collectively, our research indicates that TTN, GDF15, and MAPK14 can serve as prognostic biomarkers in female KIRC patients, offering prospects for enhanced treatment and patient outcomes in these cancers.

Indexed as

ccRCCGender differencesKIRCProlactin signaling pathwayTTN

Identifiers

PMID40854626
PMCPMC12169730

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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.