Observational studyBMC gastroenterology2025
Clinical significance of the S204 phosphorylation of the Smad3 protein in combination with Ki67 for the metastasis and prognosis of gastric cancer.
Observational study in BMC gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- ETV4 as a potential target gene for alleviating proliferation metastasis of HCC.BMC gastroenterology · 2026Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
aimThe purpose of this study is to explore the prognostic evaluation value of Ki67 and pSmad3L (S204) for gastric cancer (GC) patients by jointly analyzing their expression levels in GC tissues.
methodsThis single-center observational study enrolled 98 patients with pathologically confirmed GC, collecting 82 paired samples of tumor and adjacent normal tissues. Immunohistochemistry was utilized to detect the expression levels of CD133, E-cad, Ki67, and pSmad3L (S204). Pearson correlation coefficients were calculated to assess inter-protein relationships, while chi-square tests evaluated associations with clinicopathological parameters. Kaplan-Meier analysis generated survival curves, and univariate and multivariate COX regression analyses were conducted to establish a prognostic prediction model.
resultsCompared with adjacent normal tissues, the expressions of CD133, E-cad, and Ki67 were upregulated in GC tissues. The high expression of CD133 was associated with the tumor type, and the high expression of Ki67 was related to tumor grading and distant metastasis. Multivariate analysis showed that the depth of invasion, lymph node metastasis, Ki67, and pSmad3L (S204) were independent prognostic risk factors for GC patients. The co-expression of high levels of Ki67 and pSmad3L (S204) predicted a poor prognosis.
conclusionHigh expression of Ki67 and high expression of pSmad3L(S204) are independent risk factors for the prognosis of patients with GC, and the combined analysis of Ki67 and pSmad3L(S204) can help to improve the risk prediction.
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