Overexpression of ASAP1 is associated with poor prognosis in epithelial ovarian cancer

被引:2
作者
Hou, Teng [1 ]
Yang, Chenlu [1 ]
Tong, Chongjie [1 ]
Zhang, Huiting [1 ]
Xiao, Juan [1 ]
Li, Jundong [1 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou 510060, GD, Peoples R China
关键词
ASAP1; prognosis; epithelial ovarian cancer; GTPASE-ACTIVATING PROTEIN; CELL MOTILITY; ARF1; TRAFFICKING; EXPRESSION; GAP; PHOSPHORYLATION; METASTASIS; SURVIVAL; PROVIDES;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: This study was conducted to analyze the clinical significance of ASAP1 in epithelial ovarian cancer (EOC). Methods: A total of 95 patients with EOC were included in the study. The expression profile of ASAP1 in 10 pairs of ovarian cancer and normal ovary tissues were detected by Real-time PCR. The expression level of ASAP1 in 95 paraffin-embedded EOC specimens was measured by immunohistochemistry staining. Statistical analysis was performed to evaluate the clinicopathologic significance of ASAP1. Results: Levels of ASAP1 mRNA were higher in EOC than in normal ovary tissues. Patients with higher ASAP1 expression had shorter overall (P=0.019) and recurrence-free (P=0.030) survival time, whereas those with lower ASAP1 expression survived longer. In addition, high expression of ASAP1 was correlated with poor overall (P=0.044) and recurrence-free (P=0.006) survival in patients with advanced carcinomas. Moreover, statistical analysis displayed a significant correlation in ASAP1 expression with pelvic metastasis (P=0.015). Multivariate analysis revealed that an elevated ASAP1 expression was a significant independent prognostic factor for the overall (P=0.039) and recurrence-free (P=0.028) survival of EOC patients. Conclusion: These results indicated that elevated expression of ASAP1 plays an important role in the progression and metastasis of ovarian cancer, and that ASAP1 may be used as a biomarker in predicting patient outcome in EOC patients.
引用
收藏
页码:280 / 287
页数:8
相关论文
共 28 条
[21]   CrkL directs ASAP1 to peripheral focal adhesions [J].
Oda, A ;
Wada, I ;
Miura, K ;
Okawa, K ;
Kadoya, T ;
Kato, T ;
Nishihara, H ;
Maeda, M ;
Tanaka, S ;
Nagashima, K ;
Nishitani, C ;
Matsuno, K ;
Ishino, M ;
Machesky, LM ;
Fujita, H ;
Randazzo, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6456-6460
[22]   Expression of AMAP1, an ArfGAP, provides novel targets to inhibit breast cancer invasive activities [J].
Onodera, Y ;
Hashimoto, S ;
Hashimoto, A ;
Morishige, M ;
Mazaki, Y ;
Yamada, A ;
Ogawa, E ;
Adachi, M ;
Sakurai, T ;
Manabe, T ;
Wada, H ;
Matsuura, N ;
Sabe, H .
EMBO JOURNAL, 2005, 24 (05) :963-973
[23]   Revised FIGO staging for carcinoma of the cervix [J].
Pecorelli, Sergio ;
Zigliani, Lucia ;
Odicino, Franco .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2009, 105 (02) :107-108
[24]   Arf GAPs: multifunctional proteins that regulate membrane traffic and actin remodelling [J].
Randazzo, PA ;
Hirsch, DS .
CELLULAR SIGNALLING, 2004, 16 (04) :401-413
[25]  
Schwartz Peter E, 2002, Cancer Treat Res, V107, P99
[26]   GEFH1 binds ASAP1 and regulates podosome formation [J].
Shiba, Yoko ;
Randazzo, Paul A. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 406 (04) :574-579
[27]  
Siegel RL, 2020, ANTI-CANCER DRUG, V70, P7, DOI [10.3322/caac.21590, DOI 10.1097/CAD.0000000000000617]
[28]   The Arf GAP ASAP1 provides a platform to regulate Arf4-and Rab11-Rab8-mediated ciliary receptor targeting [J].
Wang, Jing ;
Morita, Yoshiko ;
Mazelova, Jana ;
Deretic, Dusanka .
EMBO JOURNAL, 2012, 31 (20) :4057-4071