Standard of Care and Promising New Agents for the Treatment of Mesenchymal Triple-Negative Breast Cancer

被引:12
作者
Mezi, Silvia [1 ]
Botticelli, Andrea [2 ]
Pomati, Giulia [3 ]
Cerbelli, Bruna [1 ]
Scagnoli, Simone [4 ]
Amirhassankhani, Sasan [5 ]
d'Amati, Giulia [1 ]
Marchetti, Paolo [2 ]
机构
[1] Univ Rome Sapienza, Dept Radiol Oncol & Pathol Sci, I-00185 Rome, Italy
[2] Univ Rome Sapienza, Dept Clin & Mol Med, I-00185 Rome, Italy
[3] Univ Rome Sapienza, Dept Mol Med, I-00185 Rome, Italy
[4] Univ Rome Sapienza, Dept Med & Surg Sci & Translat Med, I-00185 Rome, Italy
[5] Guys & St Thomas NHS Fdn Trust, Dept Plast Surg, London SE1 7EH, England
关键词
triple negative; breast cancer; mesenchymal subtype; immunotherapy; target therapy;
D O I
10.3390/cancers13051080
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Mesenchymal triple negative breast cancer subtype expresses genes involved in proliferation, epithelial to mesenchymal transition, stromal interaction and cell motility. Moreover, this subgroup is characterized by an immunosuppressive microenvironment. This review focuses on the intracellular pathways involved in tumorigenesis and cancer progression, as well as in the immune evasion mechanisms. Furthermore, we provide an overview of current clinical trials investigating the efficacy and safety of different therapeutic molecules for this aggressive subtype of triple negative breast cancer. The challenge is to restore immunocompetence by overcoming the chemo and immune-resistance profile of mesenchymal triple negative breast cancer to achieve a lasting response to therapy. The pathologic definition of triple negative breast cancer (TNBC) relies on the absence of expression of estrogen, progesterone and HER2 receptors. However, this BC subgroup is distinguished by a wide biological, molecular and clinical heterogeneity. Among the intrinsic TNBC subtypes, the mesenchymal type is defined by the expression of genes involved in the epithelial to mesenchymal transition, stromal interaction and cell motility. Moreover, it shows a high expression of genes involved in proliferation and an immune-suppressive microenvironment. Several molecular alterations along different pathways activated during carcinogenesis and tumor progression have been outlined and could be involved in immune evasion mechanisms. Furthermore, reverting epithelial to mesenchymal transition process could lead to the overcoming of immune-resistance. This paper reviews the current knowledge regarding the mesenchymal TNBC subtype and its response to conventional therapeutic strategies, as well as to some promising molecular target agents and immunotherapy. The final goal is a tailored combination of cytotoxic drugs, target agents and immunotherapy in order to restore immunocompetence in mesenchymal breast cancer patients.
引用
收藏
页码:1 / 24
页数:24
相关论文
共 103 条
[1]   Bidirectional crosstalk between PD-L1 expression and epithelial to mesenchymal transition: Significance in claudin-low breast cancer cells [J].
Alsuliman, Abdullah ;
Colak, Dilek ;
Al-Harazi, Olfat ;
Fitwi, Hanaa ;
Tulbah, Asma ;
Al-Tweigeri, Taher ;
Al-Alwan, Monther ;
Ghebeh, Hazem .
MOLECULAR CANCER, 2015, 14
[2]  
[Anonymous], PRIM RES IMPASSION13
[3]  
[Anonymous], IP IPAT PACL PAC PIK
[4]  
ASSOIAN RK, 1983, J BIOL CHEM, V258, P7155
[5]  
AWADA A, 2013, J CLIN ONCOL, V31
[6]   Sacituzumab Govitecan-hziy in Refractory Metastatic Triple-Negative Breast Cancer [J].
Bardia, A. ;
Mayer, I. A. ;
Vahdat, L. T. ;
Tolaney, S. M. ;
Isakoff, S. J. ;
Diamond, J. R. ;
O'Shaughnessy, J. ;
Moroose, R. L. ;
Santin, A. D. ;
Abramson, V. G. ;
Shah, N. C. ;
Rugo, H. S. ;
Goldenberg, D. M. ;
Sweidan, A. M. ;
Iannone, R. ;
Washkowitz, S. ;
Sharkey, R. M. ;
Wegener, W. A. ;
Kalinsky, K. .
NEW ENGLAND JOURNAL OF MEDICINE, 2019, 380 (08) :741-751
[7]   Unravelling triple-negative breast cancer molecular heterogeneity using an integrative multiomic analysis [J].
Bareche, Y. ;
Venet, D. ;
Ignatiadis, M. ;
Aftimos, P. ;
Piccart, M. ;
Rothe, F. ;
Sotiriou, C. .
ANNALS OF ONCOLOGY, 2018, 29 (04) :895-902
[8]   Phase II and tumor pharmacodynamic study of gefitinib in patients with advanced breast cancer [J].
Baselga, J ;
Albanell, J ;
Ruiz, A ;
Lluch, A ;
Gascón, P ;
Guillém, V ;
González, S ;
Sauleda, S ;
Marimón, I ;
Tabernero, JM ;
Koehler, MT ;
Rojo, F .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (23) :5323-5333
[9]   Comparative Effectiveness of an mTOR-Based Systemic Therapy Regimen in Advanced, Metaplastic and Nonmetaplastic Triple-Negative Breast Cancer [J].
Basho, Reva K. ;
Yam, Clinton ;
Gilcrease, Michael ;
Murthy, Rashmi K. ;
Helgason, Thorunn ;
Karp, Daniel D. ;
Meric-Bernstam, Funda ;
Hess, Kenneth R. ;
Valero, Vicente ;
Albarracin, Constance ;
Litton, Jennifer K. ;
Chavez-MacGregor, Mariana ;
Hong, David ;
Kurzrock, Razelle ;
Hortobagyi, Gabriel N. ;
Janku, Filip ;
Moulder, Stacy L. .
ONCOLOGIST, 2018, 23 (11) :1300-1309
[10]   Targeting the PI3K/AKT/mTOR Pathway for the Treatment of Mesenchymal Triple-Negative Breast Cancer Evidence From a Phase 1 Trial of mTOR Inhibition in Combination With Liposomal Doxorubicin and Bevacizumab [J].
Basho, Reva K. ;
Gilcrease, Michael ;
Murthy, Rashmi K. ;
Helgason, Thorunn ;
Karp, Daniel D. ;
Meric-Bernstam, Funda ;
Hess, Kenneth R. ;
Herbrich, Shelley M. ;
Valero, Vicente ;
Albarracin, Constance ;
Litton, Jennifer K. ;
Chavez-MacGregor, Mariana ;
Ibrahim, Nuhad K. ;
Murray, James L., III ;
Koenig, Kimberly B. ;
Hong, David ;
Subbiah, Vivek ;
Kurzrock, Razelle ;
Janku, Filip ;
Moulder, Stacy L. .
JAMA ONCOLOGY, 2017, 3 (04) :509-515