Negative Expression of CPSF2 Predicts a Poorer Clinical Outcome in Patients with Papillary Thyroid Carcinoma

被引:14
|
作者
Sung, Tae Yon [1 ]
Kim, Mijin [2 ]
Kim, Tae Yong [2 ]
Kim, Won Gu [2 ]
Park, Yangsoon [3 ]
Song, Dong Eun [3 ]
Park, Su-Yeon [2 ]
Kwon, Hyemi [2 ]
Choi, Yun Mi [2 ]
Jang, Eun Kyung [2 ]
Jeon, Min Ji [2 ]
Shong, Young Kee [2 ]
Hong, Suck Joon [1 ]
Kim, Won Bae [2 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Surg, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Internal Med, Seoul 138736, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pathol, Seoul 138736, South Korea
关键词
POLYADENYLATION SPECIFICITY FACTOR; BRAF V600E MUTATION; BRAF(V600E) MUTATION; PROGNOSTIC-FACTORS; CANCER; ASSOCIATION; POPULATION; RECURRENCE; CLEAVAGE; SUBUNIT;
D O I
10.1089/thy.2015.0079
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The BRAF(V600E) mutation is a promising prognostic biomarker for patients with papillary thyroid carcinoma (PTC), but its prevalence differs widely among different geographic regions. A recent study reported that loss of the Cleavage and Polyadenylation Specificity Factor Subunit 2 (CPSF2) gene was associated with increased cellular invasion, cancer stem cells, and aggressiveness of PTC. This study aimed at evaluating CPSF2 protein expression as a prognostic marker for PTC in a region with a high prevalence of the BRAF(V600E) mutation, Korea. Methods: This study included 159 patients with classical PTC who underwent a total thyroidectomy and received ablative doses of I-131. The expression of CPSF2 protein was evaluated by immunohistochemistry and graded semi-quantitatively. The presence of the BRAF(V600E) mutation was evaluated by direct sequencing. Results: Negative protein expression of CPSF2 was observed in 34 (21.3%) of the 159 PTCs. In multivariate analysis, negative CPSF2 expression was significantly associated with cervical lymph node metastasis (odds ratio [OR]=2.56, p=0.28), and distant metastasis (OR=3.48, p=0.02). After adjusting for age, sex, tumor size, extrathyroidal invasion, lymphovascular invasion, and the BRAF(V600E) mutation, the CPSF2-negative group had a significantly lower recurrence-free survival compared to the CPSF2-positive group (hazard ratio=2.14, p=0.03). Conclusion: Negative protein expression of CPSF2 is independently associated with a poor clinical outcome in PTC. CPSF2 could be a useful prognostic marker for PTC in regions with a high prevalence of the BRAF(V600E) mutation.
引用
收藏
页码:1020 / 1025
页数:6
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