Downregulation of PDGF-D Inhibits Proliferation and Invasion in Breast Cancer MDA-MB-231 Cells

被引:11
作者
Lu, Jing-Feng [1 ]
Hu, Zhi-Qiu [1 ]
Yang, Meng-Xuan [1 ]
Liu, Wei-Yan [1 ]
Pan, Gao-Feng [1 ]
Ding, Jun-Bin [1 ]
Liu, Jia-Zhe [1 ]
Tang, Lang [2 ]
Hu, Bin [2 ]
Li, Hong-Chang [1 ]
机构
[1] Fudan Univ, Minhang Hosp, Inst Fudan Minhang Acad Hlth Syst, Dept Gen Surg, 170 Xinsong Rd, Shanghai 201100, Peoples R China
[2] Fudan Univ, Minhang Hosp, Inst Fudan Minhang Acad Hlth Syst, Dept Ultrasonog Dept, 170 Xinsong Rd, Shanghai 201100, Peoples R China
基金
中国国家自然科学基金;
关键词
Breast carcinoma; Migration; PDGF-D; Proliferation; Apoptosis; EPITHELIAL-MESENCHYMAL TRANSITION; GROWTH; RECEPTORS; PROGNOSIS; SYSTEM;
D O I
10.1016/j.clbc.2021.06.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study demonstrated that silencing of PDGF-D could inhibit breast cancer cells proliferation, increase the apoptosis rate, and inhibit cell metastasis. These results suggested that PDGF-D gene may involve in the occurrence and development of breast cancer. Background: The platelet derived growth factor-D (PDGF-D) plays an important role in breast tumor aggressiveness. However, limited study has investigated the effect of silencing PDGF-D on the biological function of breast cancer. The purpose of this study is to clarify the potential value of PDGF-D as a target for breast cancer treatment. Methods: Reverse transcription-polymerase chain reaction and western blot were used to detect PDGF-D expression in 5 different breast cancer cells. The lentiviral vector was usd to silence PDGF-D in MDA-MB-231 cells. Then, Methyl Thiazolyl Tetrazolium was used to detect cell viability, 5-Ethynyl-2'- deoxyuridine and a soft agar assay were used to detect cell proliferation and clonality. Additionally, cell apoptosis after PDGF-D knockdown was measured by Annexin V/ Prodium Iodide staining, and cell migration was detected by trans-well assay. Survival rate and tumor size were measured by nude mice transplantation. Results: The MDA-MB-231 and SK-BR-3 cell lines showed higher PDGF-D expression than the MCF7 cell lines (P < .05). After the PDGF-D gene was silenced, the growth and colony forming abilitys ignificantly decreased (P < .05) together with the induction of apoptosis in MDA-MB-231 cells (P < .05). Moreover, MDA-MB-231 cells with PDGF-D silencing showed significantly diminished aggressive migration and invasion potential compared to other cells (P < .05). In vivo experiments also indicated that PDGF-D silencing inhibited tumor growth and improved the survival rate of tumor-bearing mice. Conclusion: Downregulation of PDGF-D had dramatic effects on breast cancer cell proliferation, apoptosis and migration, which indicates that it plays an important role in breast cancer development and progression. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:E173 / E183
页数:11
相关论文
共 27 条
[1]   PDGF family function and prognostic value in tumor biology [J].
Bartoschek, Michael ;
Pietras, Kristian .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 503 (02) :984-990
[2]   Platelet-derived growth factor-D enables liver myofibroblasts to promote tumor lymphangiogenesis in cholangiocarcinoma [J].
Cadamuro, Massimiliano ;
Brivio, Simone ;
Mertens, Joachim ;
Vismara, Marta ;
Moncsek, Anja ;
Milani, Chiara ;
Fingas, Christian ;
Malerba, Maria Cristina ;
Nardo, Giorgia ;
Dall'Olmo, Luigi ;
Milani, Eleonora ;
Mariotti, Valeria ;
Stecca, Tommaso ;
Massani, Marco ;
Spirli, Carlo ;
Fiorotto, Romina ;
Indraccolo, Stefano ;
Strazzabosco, Mario ;
Fabris, Luca .
JOURNAL OF HEPATOLOGY, 2019, 70 (04) :700-709
[3]   C-reactive protein can upregulate VEGF expression to promote ADSC-induced angiogenesis by activating HIF-1α via CD64/PI3k/Akt and MAPK/ERK signaling pathways [J].
Chen, JiaYuan ;
Gu, ZhenJie ;
Wu, MaoXiong ;
Yang, Ying ;
Zhang, JianHua ;
Ou, JingSong ;
Zuo, ZhiYi ;
Wang, JingFeng ;
Chen, YangXin .
STEM CELL RESEARCH & THERAPY, 2016, 7
[4]   Subpixel edge extraction of part ant colony optimization-based and dimensional measurement [J].
Gong, Lixiong ;
Kong, Xiangsheng ;
Liu, Yong ;
Huang, Min .
Computer Modelling and New Technologies, 2014, 18 (05) :240-246
[5]   Effect of PDGF-B aptamer on PDGFRβ/PDGF-B interaction: Molecular dynamics study [J].
Cong Quang Vu ;
Rotkrua, Pichayanoot ;
Soontornworajit, Boonchoy ;
Tantirungrotechai, Yuthana .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2018, 82 :145-156
[6]   Epithelial-mesenchymal transition in breast cancer lines is mediated through PDGF-D released by tissue-resident stem cells [J].
Devarajan, Eswaran ;
Song, Yao-Hua ;
Krishnappa, Srinivasalu ;
Alt, Eckhard .
INTERNATIONAL JOURNAL OF CANCER, 2012, 131 (05) :1023-1031
[7]   Platelet-derived growth factor (PDGF) signalling in cancer: rapidly emerging signalling landscape [J].
Farooqi, Ammad Ahmad ;
Siddik, Zahid H. .
CELL BIOCHEMISTRY AND FUNCTION, 2015, 33 (05) :257-265
[8]   PDGF-C and PDGF-D signaling in vascular diseases and animal models [J].
Folestad, Erika ;
Kunath, Anne ;
Wagsater, Dick .
MOLECULAR ASPECTS OF MEDICINE, 2018, 62 :1-11
[9]   The PDGF pathway in breast cancer is linked to tumour aggressiveness, triple-negative subtype and early recurrence [J].
Jansson, Sara ;
Aaltonen, Kristina ;
Bendahl, Par-Ola ;
Falck, Anna-Karin ;
Karlsson, Maria ;
Pietras, Kristian ;
Ryden, Lisa .
BREAST CANCER RESEARCH AND TREATMENT, 2018, 169 (02) :231-241
[10]   Platelet-derived growth factor-D promotes colorectal cancer cell migration, invasion and proliferation by regulating Notch1 and matrix metalloproteinase-9 [J].
Jiang, Bin ;
Chen, Jinhuang ;
Yuan, Wenzheng ;
Ji, Jintong ;
Liu, Zhengyi ;
Wu, Liang ;
Tang, Qiang ;
Shu, Xiaogang .
ONCOLOGY LETTERS, 2018, 15 (02) :1573-1579