Evidence map›Paper›PMID 40365941›Full record

ArticlePathology international2025

Kidney Injury Molecule-1 Expression in Pathological T1b Clear Cell Renal Cell Carcinoma: A Putative Biomarker of High Immune-Inflamed Status and Recurrence.

Ayuna Sugai, Kosuke Miyai, Keiichi Ito, Susumu Matsukuma, Kimiya Sato

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Article in Pathology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ayuna SugaiDepartment of Basic Pathology, National Defense Medical College, Tokorozawa, Japan.
Kosuke MiyaiDepartment of Basic Pathology, National Defense Medical College, Tokorozawa, Japan.ORCID https://orcid.org/0000-0003-1776-3541
Keiichi ItoDepartment of Urology, National Defense Medical College, Tokorozawa, Japan.
Susumu MatsukumaDepartment of Laboratory Medicine, National Defense Medical College Hospital, National Defense Medical College, Tokorozawa, Japan.
Kimiya SatoDepartment of Basic Pathology, National Defense Medical College, Tokorozawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kidney injury molecule-1 (KIM-1) is a potential prognostic marker of advanced-stage clear cell renal cell carcinoma (ccRCC) and is associated with tumor immunogenicity. Little is known about its role in early-stage ccRCC, especially in pathological T1b (pT1b) disease, which shows a higher recurrence rate than pT1a disease. Resected specimens from 112 pT1b ccRCC cases were reviewed and immunohistochemically analyzed for KIM-1 expression. High membranous KIM-1 expression was defined as H score ≥ 140, based on the immunoreactive intensity and area, and cytoplasmic expression in ≥ 10% of cancer cells was considered as high cytoplasmic KIM-1 expression. KIM-1 expression status was compared with clinicopathological variables, including tumor-associated immune cell (TAIC) status. Among the 112 cases, high membranous and cytoplasmic KIM-1 expression was observed in 30 (27%) and 38 (34%) cases, respectively. High membranous KIM-1 expression was significantly associated with a higher nuclear grade, tumor necrosis, hot TAIC status, and shorter recurrence-free survival (RFS) and cancer-specific survival, whereas high cytoplasmic expression was only related to a higher nuclear grade. Multivariate Cox regression analysis revealed that high membranous KIM-1 expression and tumor necrosis were independent predictors of shorter RFS. Our results indicate that membranous KIM-1 expression could be a biomarker for predicting postnephrectomy recurrence in pT1b ccRCC.

Indexed as

Biomarkers, TumorCarcinoma, Renal CellHepatitis A Virus Cellular Receptor 1Kidney NeoplasmsNeoplasm Recurrence, LocalAdultAgedAged, 80 and overFemaleHumansImmunohistochemistryMaleMiddle AgedPrognosisBiomarkers, TumorHAVCR1 protein, humanHepatitis A Virus Cellular Receptor 1cancer‐specific survivalclear cell renal cell carcinomaimmunohistochemistrykidney injury molecule‐1recurrencetumor‐associated immune cell

Identifiers

PMID40365941
PMCPMC12288442

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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.