Evidence map›Paper›PMID 30382527›Full record

ArticlePathology oncology research : POR2020

Expression of TOMM34 and Its Clinicopathological Correlations in Urothelial Carcinoma of the Bladder.

Mohamed A H Ahmed, Mohamed Hassan Ali, Hashem Hafez Abbas, Gamal Ali Elatrash, Abd AlRahman Mohammad Foda

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Article in Pathology oncology research : POR, 2020. 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
0.5field-weighted citation impact, top 31% 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

5 authors at 2 institutions in 2 countries.

Mohamed A H AhmedDepartment of Pathology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Mohamed Hassan AliDepartment of Urology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Hashem Hafez AbbasDepartment of Urology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Gamal Ali ElatrashDepartment of Urology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Abd AlRahman Mohammad FodaDepartment of Pathology, Faculty of Medicine, Mansoura University, Mansoura, 35516, Egypt. abdofoda@mans.edu.eg.ORCID http://orcid.org/0000-0002-6858-9822
Suez Canal University · EGMansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The substantial difference between normal cells and cancer cells in terms of their energy metabolism in mitochondria provides an interesting basis for the development of novel therapeutic agents targeting energy machinery of tumour cells. TOMM34 is one of the Tom (translocase of the outer membrane of mitochondria) family that was found to be overexpressed in colorectal, hepatocellular, lung and early invasive breast carcinomas. The expression profile of mitochondrial translocases in bladder cancer compared to normal urinary bladder tissues has not been investigated yet. Therefore, the aim of the current study is to investigate the expression pattern of TOMM34 in bladder cancer tissues and explore its correlation with the clinico-pathological parameters of those cases. Sixty patients who underwent either transurethral resection or radical cystectomy for bladder cancer were included in this study with revision of all their clinicopathological data and tumor slides. Ten histologically normal urothelial biopsies were also included. Immunohistochemical staining for TOMM34 was done and semi-quantitatively scored using the modified H-score. All relations were analysed using established statistical methodologies. TOMM34 overexpression was significantly associated with high tumour stage, muscle invasion and high grade. Significant positive association was observed between TOMM34 expression and poor outcome in terms of shorter disease-specific survival. This study suggests TOMM34 as a biomarker of progression and poor prognosis in urothelial cell carcinoma patients. Furthermore, we suggest a role played by mitochondrial machinery in urothelial cell carcinoma progression, which is a potential target for the newly-discovered vaccine therapy for urothelial cell carcinoma.

Indexed as

AgedAged, 80 and overBiomarkers, TumorCarcinoma, Transitional CellDisease ProgressionFemaleHumansMaleMiddle AgedMitochondrial Membrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsPrognosisUrinary Bladder NeoplasmsBiomarkers, TumorMitochondrial Membrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsTOMM34 protein, humanMarkersMitochondrialTOMM34Urothelial

Identifiers

PMID30382527
OpenAlexW2898889135

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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.