论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
Authors Zhang Y, Huang F, Luo Q, Wu X, Liu Z, Chen H, Huang Y
Received 13 April 2018
Accepted for publication 2 October 2018
Published 5 December 2018 Volume 2018:11 Pages 8751—8759
DOI https://doi.org/10.2147/OTT.S171053
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Andrew Yee
Peer reviewer comments 3
Editor who approved publication: Prof. Dr. Geoffrey Pietersz
Purpose: Carboplatin is
a first-line treatment for ovarian cancer. However, most patients develop
resistance and undergo disease recurrence. This study aims to explore the
relationship between the expression of X-linked inhibitor of apoptosis protein
(XIAP) and carboplatin sensitivity in ovarian cancer.
Patients and methods: We
examined the expression of XIAP in ovarian cancer by immunochemistry. Next, we
investigated the role of XIAP in regulating carboplatin sensitivity in ovarian
cancer ES2 and 3AO cells through Cell Counting Kit-8 cell viability assay and
fluorescein isothiocyanate-Annexin V/propidium iodide apoptosis assay.
Expression of apoptotic effectors was measured by Western blot.
Results: The
immunochemistry results showed that high XIAP expression levels inversely
correlated with carboplatin response (P =0.03) and progression-free survival (P =0.0068) in
patients with ovarian cancer. Knockdown of XIAP repressed the cell viabilities
in the carboplatin-treated cells and increased carboplatin-induced caspase
activation. In summary, our data show that XIAP mediates carboplatin
sensitivity of ovarian cancer.
Conclusion: In
summary, our data show that XIAP mediates carboplatin sensitivity of ovarian
cancer and XIAP may be a novel target for the treatment of
carboplatin-resistant ovarian cancer.
Keywords: XIAP,
carboplatin, chemosensitivity, ovarian cancer
