TRPV6 is a prognostic marker in early-stage cervical squamous cell carcinoma

被引:7
作者
Sun, Fei [1 ]
Xiao, Lu [1 ]
Jang, Xin-Xing [2 ]
Xiong, Ying [3 ]
Li, Qi [2 ]
Yue, Xiao-jing [1 ]
Wei, Yun-Jian [2 ]
Wei, Yan-Xing [1 ]
Ma, Yan-Lin [1 ,2 ]
Yu, Yan-Hong [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Obstet & Gynecol, 1838 North Guangzhou Ave, Guangzhou 510515, Guangdong, Peoples R China
[2] Hainan Med Univ, Affiliated Hosp, Hainan Prov Key Lab Human Reprod Med & Genet Res, Haikou 571101, Hainan, Peoples R China
[3] Sun Yat Sen Univ, Dept Gynecol Oncol, Ctr Canc, 651 Dongfeng Rd East, Guangzhou 510060, Guangdong, Peoples R China
基金
中国国家自然科学基金; 对外科技合作项目(国际科技项目);
关键词
TRPV6; Early-stage squamous cell cervical carcinoma; Prognosis; Biomarker; RADICAL HYSTERECTOMY; PELVIC LYMPHADENECTOMY; PROSTATE-CANCER; CATION CHANNEL; EXPRESSION; RECEPTOR;
D O I
10.1007/s13277-016-5368-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Transient receptor potential vanilloid 6 (TRPV6) has been shown to promote caner proliferation in several solid tumors, leading to unfavorable clinical outcomes. Our study aimed to elucidate the clinical significance of TRPV6 in patients with early-stage cervical squamous cell carcinoma (CSCC). The mRNA expression of TRPV6 was measured in 12 paired early-stage CSCC specimens and six cervical carcinoma cell lines using quantitative real-time PCR (qRT-PCR). Western blotting and immunohistochemistry (IHC) were employed to examine the protein expression level of TRPV6 in four paired specimens, 175 paraffin-embedded early-stage CSCC specimens, and 50 normal cervical tissues (NCTs), respectively. Statistical analyses were performed to evaluate the clinical significance of TRPV6 expression. The expressions of TRPV6 mRNA and protein were both significantly downregulated in early-stage CSCC tissues and cervical cancer cell lines. IHC analyses revealed that TRPV6 was downregulated in 136 (77.7 %) of 175 early-stage CSCC specimens. Moreover, TRPV6 expression in early-stage CSCC was significantly correlated with the tumor stage (P < 0.001), tumor growth type (P < 0.001), tumor size (P = 0.008), and differentiation grade (P = 0.003). The early-stage CSCC patients with a low TRPV6 expression level had a short progress-free survival (PFS) and overall survival (OS) duration. Univariate and multivariate analyses identified TRPV6 as an independent prognostic factor for early-stage CSCC patients' survival. We demonstrated that TRPV6 was downregulated in CSCC, which was correlated with unfavorable survival outcomes of early-stage CSCC patients. TRPV6 may be used as a novel prognostic marker for early-stage CSCC.
引用
收藏
页码:15743 / 15751
页数:9
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