High phospho-histone H3 expression uniquely predicts favorable survival among four markers of cellular proliferation in colorectal cancer
- PMID: 33631042
- DOI: 10.1111/pin.13084
High phospho-histone H3 expression uniquely predicts favorable survival among four markers of cellular proliferation in colorectal cancer
Abstract
Colorectal cancer (CRC) is one of the most frequent gastrointestinal cancers worldwide, with high morbidity and mortality rates. Despite numerous attempts to identify prognostic markers for the CRC patients, the significance of the association of cellular proliferation markers with survival is controversial. Here we used immunohistochemistry to detect four markers of cellular proliferation expressed in primary CRC tissue specimens (n = 269) to assess their potential to serve as prognostic factors. CRC cells variably expressed phospho-histone H3 (PHH3) (range, 0-76 per high-powered field (HPF); median, 7 per HPF), cyclin A (CCNA) (range, 11.3-73.7%; median, 32%), geminin (GMNN) (range, 7.8-82.0%; median, 37.1%), and marker of proliferation Ki-67 (MKI67) (range, 4.9-96.6%; median, 49.6%). Among them, patients with PHH3-high (≥7 per HPF) tumors uniquely experienced significantly longer 5-year survival than those with PHH3-low (≤6 per HPF) (81.8% vs. 65.5%; P = 0.0047). Multivariable Cox hazards regression analysis identified PHH3-high (hazard ratio, 0.54; 95% confidence interval, 0.31-0.92; P = 0.025) as potential favorable factors. PHH3 levels inversely associated with pT stage (P < 0.0001) and were significantly and inversely associated with tumor diameter (ρ = -0.314, P < 0.0001). These findings support the use of PHH3 immunohistochemistry for predicting the prognoses of patients with CRC.
Keywords: colorectal cancer; immunohistochemistry; phospho-histone H3; prognostication; proliferation markers.
© 2021 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd.
Comment in
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Editorial Comment on High phospho-histone H3 expression uniquely predicts favorable survival among four markers of cellular proliferation in colorectal cancer.Pathol Int. 2021 May;71(5):325. doi: 10.1111/pin.13097. Epub 2021 Apr 6. Pathol Int. 2021. PMID: 33823085 No abstract available.
References
REFERENCES
-
- Oh HH, Joo YE. Novel biomarkers for the diagnosis and prognosis of colorectal cancer. Intest Res 2020; 18: 168-83.
-
- Ahn C, Jeong CW, Kwak C, Kim HH, Kim HS, Ku JH. Ki-67 as a prognostic marker in upper urinary tract urothelial carcinoma: A systematic review and meta-analysis. Clin Genitourin Cancer 2018; 16: e831-41.
-
- Joshi S, Watkins J, Gazinska P et al. Digital imaging in the immunohistochemical evaluation of the proliferation markers Ki67, MCM2 and Geminin, in early breast cancer, and their putative prognostic value. BMC Cancer 2015; 15: 546.
-
- Luo G, Hu Y, Zhang Z et al. Clinicopathologic significance and prognostic value of Ki-67 expression in patients with gastric cancer: A meta-analysis. Oncotarget 2017; 8: 50273-83.
-
- Menon SS, Guruvayoorappan C, Sakthivel KM, Rasmi RR. Ki-67 protein as a tumour proliferation marker. Clin Chim Acta 2019; 491: 39-45.
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