Osteopontin and its downstream carcinogenic molecules: regulatory mechanisms and prognostic value in cancer progression

被引:14
作者
Chen, Lang [1 ]
Huan, Xuan [2 ]
Xiao, Guo-Hui [1 ]
Yu, Wu-Han [1 ]
Li, Teng-Fei [1 ]
Gao, Xi -Dan [2 ]
Zhang, You-Cheng [1 ]
机构
[1] Lanzhou Univ, Hosp 2, Hepat Biliary Pancreat Inst, Dept Gen Surg, Lanzhou, Gansu, Peoples R China
[2] Lanzhou Univ, Hosp 2, Lanzhou, Gansu, Peoples R China
关键词
osteopontin; mechanisms; oncogenic molecules; prognostic value; cancer; ENDOTHELIAL GROWTH-FACTOR; EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-TUMOR GROWTH; CELL LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; SPLICE VARIANTS; PLASMINOGEN-ACTIVATOR; MESSENGER-RNA; BETA-CATENIN; CYCLOOXYGENASE-2; EXPRESSION;
D O I
10.4149/neo_2022_220507N489
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteopontin (OPN) is a multifunctional phosphorylated glycoprotein that is expressed at significantly elevated levels in various cancers. OPN overexpression is closely associated with the development of cancer progression such as proliferation, metastasis, angiogenesis, apoptosis resistance, drug resistance, and immunosuppression, and may also be an independent prognostic biomarker for a variety of cancers. This review broadly summarizes the mechanisms that regulate the expression of downstream oncogenic molecules after OPN binds to integrin receptors or CD44 receptors, which involve a complex intracellular "signaling traffic network" (including key kinases, signaling pathways, and transcription factors). In addition, we review the prognostic value of OPN, OPN synergistic downstream oncogenic molecules in the female breast, non-small cell lung, prostate, colorectal, gastric, and hepatocellular carcinomas. The prognostic value of OPN in tissues or blood may vary due to differences in study subjects or detection methods, and this aspect of the study requires further systematization with a view to applying the detection of OPN to clinical applications. Importantly, based on the fact that the oncogenic effect of OPN correlates with the expression of the above-mentioned oncogenic molecules, this work may provide some help in the study of combination therapy targeting OPN and the above-mentioned oncogenic molecules.
引用
收藏
页码:1253 / 1269
页数:17
相关论文
共 132 条
[1]   Osteopontin selectively regulates p70S6K/mTOR phosphorylation leading to NF-κB dependent AP-1-mediated ICAM-1 expression in breast cancer cells [J].
Ahmed, Mansoor ;
Kundu, Gopal C. .
MOLECULAR CANCER, 2010, 9
[2]   Role of osteopontin as a predictive biomarker for anti-EGFR therapy in triple-negative breast cancer [J].
Anborgh, Pieter H. ;
Lee, Danny J. ;
Stam, Pieter F. ;
Tuck, Alan B. ;
Chambers, Ann F. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2018, 22 (08) :727-734
[3]  
Assidi Mourad, 2019, Tumour Biol, V41, p1010428319863627, DOI [10.1177/1010428319863627, 10.1177/1010428319863627]
[4]   Osteopontin as a therapeutic target for cancer [J].
Bandopadhyay, Monalisa ;
Bulbule, Anuradha ;
Butti, Ramesh ;
Chakraborty, Goutam ;
Ghorpade, Priyanka ;
Ghosh, Pompom ;
Gorain, Mahadeo ;
Kale, Smita ;
Kumar, Dhiraj ;
Kumar, Santosh ;
Totakura, Kumar V. S. ;
Roy, Gaurab ;
Sharma, Priyanka ;
Shetti, Dattatrya ;
Soundararajan, Gowrishankar ;
Thorat, Dhanashri ;
Tomar, Deepti ;
Nalukurthi, Radha ;
Raja, Remya ;
Mishra, Rosalin ;
Yadav, Amit S. ;
Kundu, Gopal C. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2014, 18 (08) :883-895
[5]   Activation of JAK2/STAT3 signaling by osteopontin promotes tumor growth in human breast cancer cells [J].
Behera, Reeti ;
Kumar, Vinit ;
Lohite, Kirti ;
Karnik, Swapnil ;
Kundu, Gopal C. .
CARCINOGENESIS, 2010, 31 (02) :192-200
[6]   Serial plasma osteopontin levels have prognostic value in metastatic breast cancer [J].
Bramwell, Vivien H. C. ;
Doig, Gordon S. ;
Tuck, Alan B. ;
Wilson, Sylvia M. ;
Tonkin, Katia S. ;
Tomiak, Anna ;
Perera, Francisco ;
Vandenberg, Theodore A. ;
Chambers, Ann F. .
CLINICAL CANCER RESEARCH, 2006, 12 (11) :3337-3343
[7]   Hypoxia-driven paracrine osteopontin/integrin αvβ3 signaling promotes pancreatic cancer cell epithelial-mesenchymal transition and cancer stem cell-like properties by modulating forkhead box protein M1 [J].
Cao, Junyu ;
Li, Jie ;
Sun, Liankang ;
Qin, Tao ;
Xiao, Ying ;
Chen, Ke ;
Qian, Weikun ;
Duan, Wanxing ;
Lei, Jianjun ;
Ma, Jiguang ;
Ma, Qingyong ;
Han, Liang .
MOLECULAR ONCOLOGY, 2019, 13 (02) :228-245
[8]   Osteopontin promotes a cancer stem cell-like phenotype in hepatocellular carcinoma cells via an integrin-NF-κB-HIF-1α pathway [J].
Cao, Lei ;
Fan, Xiaoyu ;
Jing, Wei ;
Liang, Yingchao ;
Chen, Rui ;
Liu, Yingying ;
Zhu, Minhui ;
Jia, Rongjie ;
Wang, Hao ;
Zhang, Xueguang ;
Zhang, Yanyun ;
Zhou, Xuyu ;
Zhao, Jian ;
Guo, Yajun .
ONCOTARGET, 2015, 6 (09) :6627-6640
[9]   Osteopontin splice variants differentially modulate the migratory activity of hepatocellular carcinoma cell lines [J].
Chae, Sujin ;
Jun, Hyoung-Oh ;
Lee, Eun Gyo ;
Yang, Suk-Jin ;
Lee, Dong Chul ;
Jung, Joon Ki ;
Park, Kyung Chan ;
Yeom, Young Il ;
Kim, Kyu-Won .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2009, 35 (06) :1409-1416
[10]   Curcumin suppresses breast tumor angiogenesis by abrogating osteopontin-induced VEGF expression [J].
Chakraborty, Goutam ;
Jain, Shalini ;
Kale, Smita ;
Raja, Remya ;
Kumar, Santosh ;
Mishra, Rosalin ;
Kundu, Gopal C. .
MOLECULAR MEDICINE REPORTS, 2008, 1 (05) :641-646