Impact of pentraxin 3 genetic variants on uterine cervical cancer clinicopathologic characteristics

被引:8
|
作者
Sun, Yi-Hung [1 ,2 ]
Chou, Ying-Hsiang [1 ,3 ,4 ]
Wang, Chun-Hao [5 ]
Hsiao, Yi-Hsuan [6 ,7 ]
Lee, Chung-Yuan [8 ,9 ]
Yang, Shun-Fa [1 ,10 ]
Wang, Po-Hui [1 ,6 ,11 ]
机构
[1] Chung Shan Med Univ, Inst Med, 110,Sect 1,Chien Kuo North Rd, Taichung 40201, Taiwan
[2] Chi Mei Fdn Med Ctr, Dept Obstet & Gynecol, Tainan, Taiwan
[3] Chung Shan Med Univ, Dept Med Imaging & Radiol Sci, Taichung, Taiwan
[4] Chung Shan Med Univ Hosp, Dept Radiat Oncol, Taichung, Taiwan
[5] Natl Taiwan Univ, Dept Med, Taipei, Taiwan
[6] Chung Shan Med Univ, Sch Med, Taichung, Taiwan
[7] Changhua Christian Hosp, Dept Obstet & Gynecol, Changhua, Taiwan
[8] Chiayi Chang Gung Mem Hosp Chiayi, Dept Obstet & Gynecol, Chiayi, Taiwan
[9] Chang Gung Univ Sci & Technol, Dept Nursing, Chiayi Campus, Chiayi, Taiwan
[10] Chung Shan Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[11] Chung Shan Med Univ Hosp, Dept Obstet & Gynecol, Taichung, Taiwan
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2021年 / 18卷 / 11期
关键词
pentraxin; 3; genetic variants; uterine cervical cancer; pelvic lymph node metastasis; INNATE IMMUNITY; LONG PENTRAXIN; PLASMA-LEVELS; PTX3; INFLAMMATION; PROTEIN; ASPERGILLOSIS; PROGNOSIS; FAMILY; RISK;
D O I
10.7150/ijms.57886
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aims of this study were to investigate the relationships among pentraxin 3 (PTX3) genetic variants and development and clinicopathological characteristics of uterine cervical cancer, and patient survival in Taiwanese women. The study enrolled 125 patients with invasive cancer and 98 patients with precancerous lesions of uterine cervix, and 325 control women. PTX3 genetic variants rs2120243, rs3816527, rs2305619 and rs1840680 were selected and their genotypic distributions were determined by real-time polymerase chain reaction. Our results indicated that patients with genotype CC in PTX3 rs2120243 and genotype GG in rs1840680 had more chance to have adenocarcinoma but not squamous cell carcinoma, as compared to those with CA/AA and those with GA/AA, respectively. No other clinicopatholgical characteristics were associated with PTX3 genetic variants. In addition, PTX3 genetic variants were not associated with 5 years survival of cervical cancer patients. In conclusions, PTX3 genetic variants are not associated with carcinogenesis and clinicopathological variables of uterine cervix and patient survival in Taiwanese women. The only independent predictor for the 5 years survival is pelvic lymph node metastasis.
引用
收藏
页码:2339 / 2346
页数:8
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