Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer

被引:122
作者
Maric, Gordana [1 ,2 ]
Rose, April A. N. [3 ]
Annis, Matthew G. [1 ,2 ]
Siegel, Peter M. [1 ,2 ,4 ,5 ]
机构
[1] McGill Univ, Goodman Canc Res Ctr, Montreal, PQ H3A 1A3, Canada
[2] McGill Univ, Dept Med, Montreal, PQ H3A 1A3, Canada
[3] McGill Univ, Fac Med, Montreal, PQ H3A 1A3, Canada
[4] McGill Univ, Dept Biochem, Montreal, PQ H3A 1A3, Canada
[5] McGill Univ, Dept Anat & Cell Biol, Montreal, PQ H3A 1A3, Canada
关键词
GPNMB; osteoactivin; breast cancer; antibody-drug conjugates; CDX-011; MELANOMA PROTEIN-B; ANTIBODY-DRUG CONJUGATE; BREAST-CANCER; DC-HIL; OSTEOBLAST DIFFERENTIATION; TRANSMEMBRANE PROTEIN; GLEMBATUMUMAB VEDOTIN; MUTATIONAL PROCESSES; MOLECULAR PORTRAITS; NEGATIVE REGULATOR;
D O I
10.2147/OTT.S44906
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Molecularly targeted therapies are rapidly growing with respect to their clinical development and impact on cancer treatment due to their highly selective anti-tumor action. However, many aggressive cancers such as triple-negative breast cancer (TNBC) currently lack well-defined therapeutic targets against which such agents can be developed. The identification of tumor-associated antigens and the generation of antibody drug-conjugates represent an emerging area of intense interest and growth in the field of cancer therapeutics. Glycoprotein non-metastatic b (GPNMB) has recently been identified as a gene that is over-expressed in numerous cancers, including TNBC, and often correlates with the metastatic phenotype. In breast cancer, GPNMB expression in the tumor epithelium is associated with a reduction in disease-free and overall survival. Based on these findings, glembatumumab vedotin (CDX-011), an antibody-drug conjugate that selectively targets GPNMB, is currently being investigated in clinical trials for patients with metastatic breast cancer and unresectable melanoma. This review discusses the physiological and potential pathological roles of GPNMB in normal and cancer tissues, respectively, and details the clinical advances and challenges in targeting GPNMB-expressing malignancies.
引用
收藏
页码:839 / 852
页数:14
相关论文
共 107 条
[61]   Differential Ly-6C expression identifies the recruited macrophage phenotype, which orchestrates the regression of murine liver fibrosis [J].
Ramachandran, Prakash ;
Pellicoro, Antonella ;
Vernon, Madeleine A. ;
Boulter, Luke ;
Aucott, Rebecca L. ;
Ali, Aysha ;
Hartland, Stephen N. ;
Snowdon, Victoria K. ;
Cappon, Andrea ;
Gordon-Walker, Timothy T. ;
Williams, Mike J. ;
Dunbar, Donald R. ;
Manning, Jonathan R. ;
van Rooijen, Nico ;
Fallowfield, Jonathan A. ;
Forbes, Stuart J. ;
Iredale, John P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (46) :E3186-E3195
[62]   Bone-related genes expressed in advanced malignancies induce invasion and metastasis in a genetically defined human cancer model [J].
Rich, JN ;
Shi, Q ;
Hjelmeland, M ;
Cummings, TJ ;
Kuan, CT ;
Bigner, DD ;
Counter, CM ;
Wang, XF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (18) :15951-15957
[63]   Microphthalmia transcription factor regulates the expression of the novel osteoclast factor GPNMB [J].
Ripoll, Vera M. ;
Meadows, Nicholas A. ;
Raggatt, Liza-Jane ;
Chang, Ming K. ;
Pettit, Allison R. ;
Cassady, Alan I. ;
Hume, David A. .
GENE, 2008, 413 (1-2) :32-41
[64]   Gpnmb is induced in macrophages by IFN-γ and lipopolysaccharide and acts as a feedback regulator of proinflammatory responses [J].
Ripoll, Vera M. ;
Irvine, Katharine M. ;
Ravasi, Timothy ;
Sweet, Matthew J. ;
Hume, David A. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (10) :6557-6566
[65]   Osteoactivin promotes breast cancer metastasis to bone [J].
Rose, April A. N. ;
Pepin, Francois ;
Russo, Caterina ;
Abou Khalil, Jad E. ;
Hallett, Michael ;
Siegell, Peter M. .
MOLECULAR CANCER RESEARCH, 2007, 5 (10) :1001-1014
[66]   ADAM10 Releases a Soluble Form of the GPNMB/Osteoactivin Extracellular Domain with Angiogenic Properties [J].
Rose, April A. N. ;
Annis, Matthew G. ;
Dong, Zhifeng ;
Pepin, Francois ;
Hallett, Michael ;
Park, Morag ;
Siegel, Peter M. .
PLOS ONE, 2010, 5 (08)
[67]   Glycoprotein Nonmetastatic B Is an Independent Prognostic Indicator of Recurrence and a Novel Therapeutic Target in Breast Cancer [J].
Rose, April A. N. ;
Grosset, Andree-Anne ;
Dong, Zhifeng ;
Russo, Caterina ;
MacDonald, Patricia A. ;
Bertos, Nicholas R. ;
St-Pierre, Yves ;
Simantov, Ronit ;
Hallett, Michael ;
Park, Morag ;
Gaboury, Louis ;
Siegel, Peter M. .
CLINICAL CANCER RESEARCH, 2010, 16 (07) :2147-2156
[68]   Osteoactivin/HGFIN: is it a tumor suppressor or mediator of metastasis in breast cancer? [J].
Rose, April A. N. ;
Siegel, Peter M. .
BREAST CANCER RESEARCH, 2007, 9 (06)
[69]   Breast cancer molecular subtypes respond differently to preoperative chemotherapy [J].
Rouzier, R ;
Perou, CM ;
Symmans, WF ;
Ibrahim, N ;
Cristofanilli, M ;
Anderson, K ;
Hess, KR ;
Stec, J ;
Ayers, M ;
Wagner, P ;
Morandi, P ;
Fan, C ;
Rabiul, I ;
Ross, JS ;
Hortobagyi, GN ;
Pusztai, L .
CLINICAL CANCER RESEARCH, 2005, 11 (16) :5678-5685
[70]   Cloning and characterization of osteoactivin, a novel cDNA expressed in osteoblasts [J].
Safadi, FF ;
Xu, J ;
Smock, SL ;
Rico, MC ;
Owen, TA ;
Popoff, SN .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2002, 84 (01) :12-26