Abstract

Ovarian cancer (OC) is a type of gynaecological malignancy with high mortality in females. Serous ovarian cancer (SOC) is a distinct subtype of OC with poor early diagnosis. Given the limitations of traditional therapies, such as chemotherapy, targeted treatment is therefore a promising therapy to improve the survival rate of SOC patients. Cyclophilin A (CYPA) is a member of Cyclophilin family and thought to participates in multiple cellular processes such as cell transduction and immune modulation. Recently, various of studies indicated that CYPA has critical impact on cancer progression. CYPA could regulate cell proliferation, invasion, and chemoresistance of multiple types of cancers. However, it is still unclear whether it could affect ovarian cancer. In this study, we demonstrated that CYPA was highly expressed in SOC tissues compared with adjacent tissues. Further, CYPA was significantly associated with clinical stage and lymphnode metastasis of SOC patients. Additionally, data indicated that knockdown of CYPA by its shRNA dramatically reduces migration and invasion capacity of SOC cells in vitro and blocks tumor metastasis in vivo. Our study investigates the involvement of CYPA in the progression and metastasis of SOC, and therefore provides CYPA as a promising therapeutic target for SOC treatment.

Highlights

  • Ovarian cancer (OC) is s the seventh most common cancer and a type of gynaecological malignancies, with high mortality in females [1,2,3]

  • We revealed that Cyclophilin A (CYPA) depletion dramatically blocked Serous ovarian cancer (SOC) cell migration and invasion and further suppressed tumor metastasis in mice

  • CYPA expression is correlated with the survival rate and clinical features of serous ovarian cancer In decades, the involvement of CYPA in the progression of multiple cancers has been widely reported

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Summary

Introduction

Ovarian cancer (OC) is s the seventh most common cancer and a type of gynaecological malignancies, with high mortality in females [1,2,3]. The majority of ovarian cancers (nearly 90%) are originated from epithelial tissues [4, 5]. Serous ovarian cancer (SOC) is a distinct histological subtype of OC, which is usually diagnosed at advanced stage [8]. Chemotherapy is the established treatment for SOC, the survival rate remains low, and it is highly anticipated that new treatments will be successfully developed [9, 10]. Therapies, such as targeted treatment and immunotherapy, are needed to combat this disease [11, 12]. Various of proteins have been found highly expressed in SOC tissues, some of which

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