Association of miR-10a expression and its rs3809783 polymorphism with postoperative incisional pain via Bcl-6/Tfh targeting in patients undergoing laparoscopic cholecystectomy

OA: closed
⚙ AI-generated summary by qwen3.7-flash, 2026-10-06 ⓘ

This paper investigated the association of miR-10a expression and its rs3809783 polymorphism with postoperative incisional pain via Bcl-6/Tfh targeting in patients undergoing laparoscopic cholecystectomy.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

⚙ AI-generated deep summary by qwen3.7-flash, 2026-10-31 · read from full text ⓘ

This study investigated the role of miR-10a and its rs3809783 polymorphism in postoperative incisional pain among patients undergoing laparoscopic cholecystectomy for acute cholecystitis. The researchers measured miR-10a levels and immune markers in gallstone mucosal tissue, finding that lower miR-10a expression was negatively correlated with pain intensity and associated with the AT genotype, which enhances Bcl-6-mediated Tfh polarization. Mechanistic exploration using a mouse model confirmed Bcl-6 as a direct target of miR-10a, linking specific genetic variants to increased inflammatory markers and complications. Relevance to endometriosis: listed as one indication for GnRH antagonists, though the paper's main focus is uterine fibroids.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

This study aimed to investigate the role of miR-10a and its rs3809783 polymorphism in postoperative incisional pain among patients undergoing laparoscopic cholecystectomy for acute cholecystitis (ACC-LC). Levels of miR-10a and immune markers (CD68, CD19, CD3, T-bet, GATA-3, IL-17A, Bcl-6) were measured in gallstone mucosal tissue, and genotyping was performed via PCR and sequencing. An incisional pain mouse model was used for mechanistic exploration. The results showed that miR-10a expression was decreased in ACC-LC patients compared with controls and was negatively correlated with pain intensity. Patients carrying the rs3809783 AT genotype exhibited lower miR-10a levels and higher pain scores than AA carriers. Among the elevated immune markers, only Bcl-6/Tfh was associated with pain severity. Further analysis confirmed Bcl-6 as a direct target of miR-10a, with the A→T substitution at rs3809783 enhancing Bcl-6-mediated Tfh polarization. This genotype was also correlated with longer anal exhaust time, higher inflammatory markers, and more complications. In conclusion, miR-10a and its rs3809783 polymorphism may serve as biomarkers for postoperative pain in ACC-LC by regulating the Bcl-6/Tfh pathway.
Full text 2,602 characters · extracted from oa-html · 3 sections · click to expand

Abstract

This study aimed to investigate the role of miR-10a and its rs3809783 polymorphism in postoperative incisional pain among patients undergoing laparoscopic cholecystectomy for acute cholecystitis (ACC-LC). Levels of miR-10a and immune markers (CD68, CD19, CD3, T-bet, GATA-3, IL-17A, Bcl-6) were measured in gallstone mucosal tissue, and genotyping was performed via PCR and sequencing. An incisional pain mouse model was used for mechanistic exploration. The results showed that miR-10a expression was decreased in ACC-LC patients compared with controls and was negatively correlated with pain intensity. Patients carrying the rs3809783 AT genotype exhibited lower miR-10a levels and higher pain scores than AA carriers. Among the elevated immune markers, only Bcl-6/Tfh was associated with pain severity. Further analysis confirmed Bcl-6 as a direct target of miR-10a, with the A→T substitution at rs3809783 enhancing Bcl-6-mediated Tfh polarization. This genotype was also correlated with longer anal exhaust time, higher inflammatory markers, and more complications. In conclusion, miR-10a and its rs3809783 polymorphism may serve as biomarkers for postoperative pain in ACC-LC by regulating the Bcl-6/Tfh pathway.

Keywords

MicroRNA; T follicular helper cells; laparoscopic cholecystectomy; polymorphism; postoperative incisional pain. AJCEI Copyright © 2026. Conflict of interest statement None. Figures

References

- - Shiihara M, Sudo Y, Matsushita N, Kubota T, Hibi Y, Osugi H, Inoue T. Preoperative difficulty assessment of interval laparoscopic cholecystectomy for gallstones. Surgery. 2024;175:1503–1507. - PubMed - - Taheri P, Moinfar Z, Varpaei HA. Comparison of the stress responses after TAP block and epidural anesthesia in patients undergoing elective laparoscopic cholecystectomy under general anesthesia: randomized clinical trial. Clin J Pain. 2023;39:319–325. - PubMed - - Zhao L, Sun Y, Zhang Z, Li H, Fu X. Expression and genetic polymorphisms of CXCR5 are associated with postoperative incisional pain in patients undergoing laparoscopic cholecystectomy. J Laparoendosc Adv Surg Tech A. 2025;35:798–804. - PubMed LinkOut - more resources Full Text Sources

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

⚙ Ask this paper AI returns verbatim quotes from the full text · source: oa-html ⓘ

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2026) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

SciLite annotations

organisms 1
transgenic mice

Source provenance

europepmc
last seen: 2026-11-08T09:52:27.483963+00:00
scilite
last seen: 2026-10-25T10:06:56.708568+00:00
unpaywall
last seen: 2026-11-11T07:04:17.060302+00:00