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Sculthorpe, Declan J; Denton, Amy; Fadhil, Wakkas; Rusnita, Dewi; Ilyas, Mohammad; Mukherjee, Abhik
High α-SMA expression in the tumor stroma is associated with adverse clinical parameters in mismatch repair-proficient colorectal cancers only Journal Article
In: Am. J. Clin. Pathol., vol. 163, no. 3, pp. 464–472, 2025.
Abstract | Links | Altmetric | Tags: biomarker analysis, colorectal cancer, digital image analysis, DNA mismatch repair, immunohistochemistry, α-SMA
@article{Sculthorpe2025-jm,
title = {High α-SMA expression in the tumor stroma is associated with adverse clinical parameters in mismatch repair-proficient colorectal cancers only},
author = {Declan J Sculthorpe and Amy Denton and Wakkas Fadhil and Dewi Rusnita and Mohammad Ilyas and Abhik Mukherjee},
doi = {10.1093/ajcp/aqae145},
year = {2025},
date = {2025-03-01},
urldate = {2025-03-01},
journal = {Am. J. Clin. Pathol.},
volume = {163},
number = {3},
pages = {464\textendash472},
publisher = {Oxford University Press (OUP)},
abstract = {OBJECTIVES: As mismatch repair status confers differential
prognosis in colorectal cancers, this study aimed to determine
associations of α-smooth muscle actin (α-SMA)
protein expression in mismatch repair-proficient (pMMR) and
mismatch repair-deficient (dMMR) colorectal tumors with
clinicopathologic and prognostic features. METHODS: Tissue
microarrays from patients with colorectal cancer, immunostained
with α-SMA, were assessed through digital image analysis. Total (n = 962), pMMR (n = 782), and dMMR (n = 156) stromal
H-scores were assessed for associations with clinicopathologic
and survival data. RESULTS: Higher α-SMA expression was correlated with pMMR status (P = 5.2223 $times$ 10-8). In the
pMMR subgroup, higher α-SMA stromal expression at the tumor periphery was correlated with higher T stage (P = .002), perineural invasion (P = .038), infiltrative tumor edge (P = .01), involved nodal status (P = .036), metastases (P = .013), synchronous metastases (P = .007), recurrence (P = .004), and both 3-year and 5-year survival (P = .018). dMMR tumors showed
no significant correlations with α-SMA staining.
CONCLUSIONS: The findings highlight that immunostaining with
α-SMA in pMMR colorectal tumors, especially at the tumor
periphery, has the potential to identify patients with adverse
prognostic features. Digital assessment of α-SMA may
offer improved objectivity, accuracy, economy of time, and risk
stratification for management.},
keywords = {biomarker analysis, colorectal cancer, digital image analysis, DNA mismatch repair, immunohistochemistry, α-SMA},
pubstate = {published},
tppubtype = {article}
}
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