P16INK4A expression might be associated with a favorable prognosis for cervical adenocarcinoma via dysregulation of the RB pathway
Abstract Previous studies have largely failed to clarify the relationship between p16 INK4A status and cervical adenocarcinoma prognosis. The current study aimed to examine the clinical and pathological significance of p16 INK4A expression in several cervical adenocarcinoma subtypes. Eighty-two samp...
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Published in | Scientific reports Vol. 11; no. 1; p. 18236 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group
14.09.2021
Nature Publishing Group UK Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Abstract
Previous studies have largely failed to clarify the relationship between p16
INK4A
status and cervical adenocarcinoma prognosis. The current study aimed to examine the clinical and pathological significance of p16
INK4A
expression in several cervical adenocarcinoma subtypes. Eighty-two samples collected from patients with cervical adenocarcinoma were formalin fixed and paraffin embedded. Next, p16
INK4A
levels were analyzed with immunohistochemistry. Additionally, the relationship between p16
INK4A
expression and clinicopathological factors as well as prognosis was evaluated. The expression of p16
INK4A
was mostly detected in all usual cervical adenocarcinoma subtypes. In the gastric type, only a few cases were positive for p16
INK4A
expression. Results of the Kaplan–Meier analysis indicated that the positive p16
INK4A
expression in tumor cells was significantly associated with favorable progression-free survival and overall survival in patients with cervical adenocarcinoma (
p
= 0.018 and
p
= 0.047, respectively, log-rank test). Our findings suggest that the status of p16
INK4A
expression may influence prognosis. Thus, p16
INK4A
expression could be used as a biomarker for improving the prognosis of patients with cervical adenocarcinoma. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-021-97703-8 |