Synergistic effects of thalidomide and cisplatin are mediated via the PI3K/AKT and JAK1/STAT3 signaling pathways in cervical cancer

被引:7
作者
Liu, Cairu [1 ]
Feng, Haiqin [1 ]
Song, Lihong [1 ]
Li, Shuirui [1 ]
Wu, Yiping [1 ]
Yang, Liping [1 ]
机构
[1] HanDan Cent Hosp, Dept Gynecol & Obstet, 59 North Congtai Rd, Handan 056008, Hebei, Peoples R China
关键词
cisplatin; thalidomide; cervical cancer; PI3K/AKT; JAK1/STAT3; CARCINOMA-CELL-LINE; EXPRESSION; ENHANCEMENT; APOPTOSIS; GROWTH; MODEL;
D O I
10.3892/or.2022.8384
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thalidomide (THD) has been found to synergize with cisplatin (DDP) in certain types of cancers; however, their combined use in the treatment of cervical cancer has not been reported to date, at least to the best of our knowledge. Thus, the present study aimed to explore the synergistic effects of THD and DDP and determine their regulatory effects on the phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) and Janus kinase 1 (JAK1)/signal transducer and activator of transcription 3 (STAT3) pathways in cervical cancer. For this purpose, 0-160 mu M THD and 0-64 mu M DDP monotherapy or in combination were used to treat the HeLa and SiHa cervical cancer cell lines. This was followed by the calculation of the combination index (CI) and 160 mu M THD and 16 mu M DDP were then used to treat the cells. Relative cell viability and apoptosis, as well as the mRNA and protein levels of PI3K, AKT, JAK1 and STAT3 were evaluated. The results revealed that THD and DDP monotherapy suppressed the viability of the HeLa and SiHa cells in a concentration-dependent manner. Moreover, THD and DDP treatment exerted a more prominent suppressive effect on the relative viability of HeLa and SiHa cells compared with DDP monotherapy at several concentration settings; further CI calculation revealed that the optimal synergistic concentrations were 160 mu M for THD and 16 mu M for DDP. Subsequently, combined treatment with THD and DDP suppressed relative cell viability, whereas it promoted cell apoptosis compared with THD or DPP monotherapy; it also inhibited the PI3K/AKT and JAK1/STAT3 signaling pathways compared with DPP or THD monotherapy in both HeLa and SiHa cells. On the whole, the present study demonstrated that THD synergizes with DDP to exert suppressive effects on cervical cancer cell lines. This synergistic action also inactivated the PI3K/AKT and JAK1/STAT3 pathways. Thus, these findings suggest that the combined use of THD and DPP may have potential for use in the treatment of cervical cancer.
引用
收藏
页数:10
相关论文
共 39 条
[11]   The PI3K/AKT signaling pathway in cancer: Molecular mechanisms and possible therapeutic interventions [J].
Khezri, Mohammad Rafi ;
Jafari, Reza ;
Yousefi, Keyvan ;
Zolbanin, Naime Majidi .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2022, 127
[12]   Curcumin Combined with Thalidomide Reduces Expression of STAT3 and Bcl-xL, Leading to Apoptosis in Acute Myeloid Leukemia Cell Lines [J].
Kian, Mahnaz Mohammadi ;
Salemi, Mahdieh ;
Bahadoran, Mohammad ;
Haghi, Atousa ;
Dashti, Nasrin ;
Mohammadi, Saeed ;
Rostami, Shahrbano ;
Chahardouli, Bahram ;
Babakhani, Davood ;
Nikbakht, Mohsen .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2020, 14 :185-194
[13]   Paclitaxel Plus Carboplatin Versus Paclitaxel Plus Cisplatin in Metastatic or Recurrent Cervical Cancer: The Open-Label Randomized Phase III Trial JCOG0505 [J].
Kitagawa, Ryo ;
Katsumata, Noriyuki ;
Shibata, Taro ;
Kamura, Toshiharu ;
Kasamatsu, Takahiro ;
Nakanishi, Toru ;
Nishimura, Sadako ;
Ushijima, Kimio ;
Takano, Masashi ;
Satoh, Toyomi ;
Yoshikawa, Hiroyuki .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (19) :2129-U151
[14]   Cervical Cancer, Version 3.2019 [J].
Koh, Wui-Jin ;
Abu-Rustum, Nadeem R. ;
Bean, Sarah ;
Bradley, Kristin ;
Campos, Susana M. ;
Cho, Kathleen R. ;
Chon, Hye Sook ;
Chu, Christina ;
Clark, Rachel ;
Cohn, David ;
Crispens, Marta Ann ;
Damast, Shari ;
Dorigo, Oliver ;
Eifel, Patricia J. ;
Fisher, Christine M. ;
Frederick, Peter ;
Gaffney, David K. ;
Han, Ernest ;
Huh, Warner K. ;
Lurain, John R., III ;
Mariani, Andrea ;
Mutch, David ;
Nagel, Christa ;
Nekhlyudov, Larissa ;
Fader, Amanda Nickles ;
Remmenga, Steven W. ;
Reynolds, R. Kevin ;
Tillmanns, Todd ;
Ueda, Stefanie ;
Wyse, Emily ;
Yashar, Catheryn M. ;
McMillian, Nicole R. ;
Scavone, Jillian L. .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2019, 17 (01) :64-84
[15]   Improved tumor-suppressive effect of OZ-001 combined with cisplatin mediated by mTOR/p70S6K and STAT3 inactivation in A549 human lung cancer cells [J].
Lee, Jeong-Hun ;
Chung, Kyung-Sook ;
Lee, Hwi-Ho ;
Ko, Dohyeong ;
Kang, Minji ;
Yoo, Ho ;
Ahn, JooHoon ;
Lee, Jae Yeol ;
Lee, Kyung-Tae .
BIOMEDICINE & PHARMACOTHERAPY, 2021, 142
[16]   HPV Vaccination and the Risk of Invasive Cervical Cancer [J].
Lei, Jiayao ;
Ploner, Alexander ;
Elfstrom, K. Miriam ;
Wang, Jiangrong ;
Roth, Adam ;
Fang, Fang ;
Sundstrom, Karin ;
Dillner, Joakim ;
Sparen, Par .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (14) :1340-1348
[17]  
Li Li, 2016, Asian Pac J Cancer Prev, V17, P2583
[18]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[19]   Cervical cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Marth, C. ;
Landoni, F. ;
Mahner, S. ;
McCormack, M. ;
Gonzalez-Martin, A. ;
Colombo, N. .
ANNALS OF ONCOLOGY, 2017, 28 :72-83
[20]   Enhancement of cisplatin sensitivity of cisplatin-resistant human cervical carcinoma cells by bryostatin 1 [J].
Mohanty, S ;
Huang, J ;
Basu, A .
CLINICAL CANCER RESEARCH, 2005, 11 (18) :6730-6737