涎腺腺样囊性癌组织色素框同源蛋白2、T细胞免疫球蛋白黏液素3表达水平及与患者临床病理特征、预后的关系
收稿日期: 2025-03-07
网络出版日期: 2025-07-02
基金资助
河北省医学科学研究课题计划(20231445)
The levels of CBX2 and TIM3 in salivary adenoid cystic carcinoma tissue and their relationship with clinical pathological features and prognosis
Received date: 2025-03-07
Online published: 2025-07-02
目的 探究涎腺腺样囊性癌(SACC)组织色素框同源蛋白2(CBX2)、T细胞免疫球蛋白黏液素3(TIM3)表达水平及与患者临床病理特征、预后的关系。 方法 选取2016年1月至2020年1月期间在河北北方学院附属第一医院接受手术治疗的SACC患者80例。采用免疫组化测定组织CBX2、TIM3表达水平;SACC组织中CBX2、TIM3的表达与预后的关系分析采用Kaplan-Meier法;SACC患者预后的影响因素采用多因素Cox回归分析。 结果 SACC组织CBX2、TIM3阳性表达率显著高于癌旁正常腺体组织(χ2 = 11.237、8.229,P < 0.05)。CBX2、TIM3表达与神经侵犯、远处转移有关(P < 0.05)。随访5年,死亡26例,存活54例,5年总体生存率为67.50%(54/80)。死亡组SACC组织CBX2、TIM3阳性表达率高于存活组(P < 0.05)。SACC组织CBX2、TIM3阳性表达患者5年生存率显著低于CBX2、TIM3阴性表达(Log Rank χ2 = 6.564、5.197,P < 0.05)。CBX2、TIM3阳性、神经侵犯、远处转移是影响SACC患者预后的危险因素(P < 0.05)。 结论 CBX2、TIM3在SACC组织中阳性表达与患者临床病理特征及预后密切相关。
关键词: 涎腺腺样囊性癌; 色素框同源蛋白2; T细胞免疫球蛋白黏液素3; 临床病理特征; 预后
张璇 , 刘振丽 , 杨永超 , 马赛 , 刘博 , 吕红娟 . 涎腺腺样囊性癌组织色素框同源蛋白2、T细胞免疫球蛋白黏液素3表达水平及与患者临床病理特征、预后的关系[J]. 实用医学杂志, 2025 , 41(12) : 1873 -1878 . DOI: 10.3969/j.issn.1006-5725.2025.12.015
Objective To investigate CBX2 and TIM3 in salivary adenoid cystic carcinoma (SACC) tissue and their relationship with clinical pathological features and prognosis. Methods 80 patients with SACC who underwent surgical treatment in the First Affiliated Hospital of Hebei North University from January 2016 to January 2020 were selected. Immunohistochemistry was used to measure CBX2 and TIM3 in tissues. The relationship between CBX2 and TIM3 in SACC tissue and prognosis was discussed though Kaplan-Meier method. The factors influencing the prognosis of SACC were discussed using multivariate Cox regression. Results The positive rates of CBX2 and TIM3 in SACC tissues were clearly higher than those in normal glandular tissues adjacent to cancer (χ2 = 11.237, 8.229, P < 0.05). The CBX2 and TIM3 were associated with nerve invasion and distant metastasis (P < 0.05). After a 5-year follow-up, 26 cases died and 54 cases survived, with an overall 5-year survival rate of 67.50% (54/80). The death group had higher positive rates of CBX2 and TIM3 in SACC tissues than the survival group (P < 0.05). Patients with positive CBX2 and TIM3 in SACC tissues had clearly lower 5-year survival rate than patients with negative CBX2 and TIM3 (Log Rank χ2 = 6.564, 5.197, P < 0.05). CBX2, TIM3 positivity, nerve invasion, and distant metastasis were risk factors affecting prognosis (P < 0.05). Conclusion The positive expression of CBX2 and TIM3 in SACC tissues is closely related to the clinical pathological features and prognosis of patients.
| 1 | SALEH E, UKWAS A. Adenoid Cystic Carcinoma of Salivary Glands: A Ten-Year Review and an Assessment of the Current Management, Surgery, Radiotherapy, and Chemotherapy[J]. Int J Otolaryngol, 2023,2023(1):1-8. doi:10.1155/2023/7401458 |
| 2 | CANTù G. Adenoid cystic carcinoma. An indolent but aggressive tumour. Part A: From aetiopathogenesis to diagnosis[J]. Acta Otorhinolaryngol Ital, 2021,41(3):206-214. doi:10.14639/0392-100x-n1379 |
| 3 | CHOWSILPA S, AN D, MALEKI Z. Adenoid cystic carcinoma cytology: Salivary gland and nonsalivary gland[J]. Diagn Cytopathol, 2020,48(12):1282-1289. doi:10.1002/dc.24573 |
| 4 | LIU X, YANG X, ZHAN C, et al. Perineural Invasion in Adenoid Cystic Carcinoma of the Salivary Glands: Where We Are and Where We Need to Go[J]. Front Oncol, 2020,10(1):1-13. doi:10.3389/fonc.2020.01493 |
| 5 | FANG Y, PENG Z, WANG Y, et al. Current opinions on diagnosis and treatment of adenoid cystic carcinoma[J]. Oral Oncol, 2022,130(1):1-15. doi:10.1016/j.oraloncology.2022.105945 |
| 6 | MICHAELIDES I, KüNZEL J, ETTL T, et al. Adenoid cystic carcinoma of the salivary glands: A pilot study of potential therapeutic targets and characterization of the immunological tumor environment and angiogenesis[J]. Eur Arch Otorhinolaryngol, 2023,280(6):2937-2944. doi:10.1007/s00405-023-07884-3 |
| 7 | XU X, LAI C, LUO J, et al. The predictive significance of chromobox family members in prostate cancer in humans[J]. Cell Oncol (Dordr), 2024,47(4):1315-1331. doi:10.1007/s13402-024-00929-7 |
| 8 | PENG L, HUANG X, QING D, et al. MiR-30a-5p inhibits cell behaviors in esophageal cancer via modulating CBX2[J]. Mutat Res, 2023,826(1):1-11. doi:10.1016/j.mrfmmm.2023.111818 |
| 9 | LU C, TAN Y. Promising immunotherapy targets: TIM3, LAG3, and TIGIT joined the party[J]. Mol Ther Oncol, 2024,32(1):2-13. doi:10.1016/j.omton.2024.200773 |
| 10 | PALACIOS LM, PEYRET V, VIANO ME, et al. TIM3 Expression in Anaplastic-Thyroid-Cancer-Infiltrating Macrophages: An Emerging Immunotherapeutic Target[J]. Biology (Basel), 2022,11(11):1-13. doi:10.3390/biology11111609 |
| 11 | BAYAT P, MAHDAVI N, YOUNESPOUR S, et al. Interactive role of miR-29, miR-93, miR-205, and VEGF in salivary adenoid cystic carcinoma[J]. Clin Exp Dent Res, 2023,9(1):112-121. doi:10.1002/cre2.678 |
| 12 | WANG J, YANG B, ZHANG X, et al. Chromobox proteins in cancer: Multifaceted functions and strategies for modulation (Review)[J]. Int J Oncol, 2023,62(3):1-12. doi:10.3892/ijo.2023.5484 |
| 13 | HU CY, LI X, ZENG T, et al. Significance of chromobox protein (CBX) expression in diffuse LBCL[J]. Gene, 2022,813(1):1-12. doi:10.1016/j.gene.2021.146092 |
| 14 | SUN R, TU X, CHAN S, et al. CBX2 Deletion Suppresses Growth and Metastasis of Colorectal Cancer by Mettl3-p38/ERK MAPK Signalling Pathway[J]. J Cancer, 2024,15(8):2123-2136. doi:10.7150/jca.92633 |
| 15 | ZHU J, LUO J E, CHEN Y, et al. Circ_0061140 knockdown inhibits tumorigenesis and improves PTX sensitivity by regulating miR-136/CBX2 axis in ovarian cancer[J]. J Ovarian Res, 2021,14(1):1-13. doi:10.1186/s13048-021-00888-9 |
| 16 | ZENG M, LI B, YANG L, et al. CBX2 depletion inhibits the proliferation, invasion and migration of gastric cancer cells by inactivating the YAP/β-catenin pathway[J]. Mol Med Rep, 2021,23(2):137-146. doi:10.3892/mmr.2020.11776 |
| 17 | LI W, SHI R, GAO Y, et al. CBX2 promotes cervical cancer cell proliferation and resistance to DNA-damaging treatment via maintaining cancer stemness[J]. J Biol Chem, 2025,301(2):1-10. doi:10.1016/j.jbc.2025.108170 |
| 18 | 朱元媛,闫洪超,刘永利,等. BTLA、LAG3和TIM3在上皮性卵巢癌组织中的表达意义[J]. 实用医学杂志,2019,35(5):698-702. |
| 19 | ZHAO L, CHENG S, FAN L, et al. TIM-3: An update on immunotherapy[J]. Int Immunopharmacol, 2021,99(1):1-13. doi:10.1016/j.intimp.2021.107933 |
| 20 | KANDEL S, ADHIKARY P, LI G, et al. The TIM3/Gal9 signaling pathway: An emerging target for cancer immunotherapy[J]. Cancer Lett, 2021,510(1):67-78. doi:10.1016/j.canlet.2021.04.011 |
| 21 | SAUER N, JANICKA N, SZLASA W, et al. TIM-3 as a promising target for cancer immunotherapy in a wide range of tumors[J]. Cancer Immunol Immunother, 2023,72(11):3405-3425. doi:10.1007/s00262-023-03516-1 |
| 22 | YANG R, SUN L, LI C F,et al. Galectin-9 interacts with PD-1 and TIM-3 to regulate T cell death and is a target for cancer immunotherapy[J]. Nat Commun, 2021,12(1):832-845. doi:10.1038/s41467-021-21099-2 |
| 23 | GARDNER A, DE MINGO PULIDO á, H?NGGI K, et al. TIM-3 blockade enhances IL-12-dependent antitumor immunity by promoting CD8+ T cell and XCR1+ dendritic cell spatial co-localization[J]. J Immunother Cancer, 2022,10(1):1-11. doi:10.1136/jitc-2021-003571 |
| 24 | 王辉,张利娟,杨芳. 半乳糖凝集素-9和T细胞免疫球蛋白黏蛋白分子3在口腔扁平苔藓和口腔鳞状细胞癌组织中的表达及临床意义[J]. 癌症进展,2020,18(6):576-579. |
| 25 | 田绣云,周美云,韩瑞,等. 涎腺腺样囊性癌的临床特征及预后分析[J]. 医学研究杂志,2023,52(6):108-111,116. |
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