Ceritinib is a novel triple negative breast cancer therapeutic agent

被引:19
|
作者
Dong, Shengli [1 ,2 ]
Yousefi, Hassan [2 ]
Van Savage, Isabella [3 ]
Okpechi, Samuel C. [2 ]
Wright, Maryl K. [3 ]
Matossian, Margarite D. [4 ]
Collins-Burow, Bridgette M. [3 ]
Burow, Matthew E. [3 ]
Alahari, Suresh K. [2 ,5 ]
机构
[1] TYK Med Inc, Huzhou 313100, Zhejiang, Peoples R China
[2] LSUHSC Sch Med, Dept Biochem & Mol Biol, New Orleans, LA 70112 USA
[3] Tulane Univ, Sch Med, New Orleans, LA 70118 USA
[4] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[5] LSUHSC Sch Med, Stanley S Scott Canc Ctr, New Orleans, LA 70112 USA
关键词
Androgen receptor; Ceritinib; Enzalutamide; Paclitaxel; RTK; ACK; AR; ANDROGEN RECEPTOR; PROSTATE-CANCER; ACTIVATION; RESISTANCE; KINASE; IDENTIFICATION; ENZALUTAMIDE;
D O I
10.1186/s12943-022-01601-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Triple-negative breast cancers (TNBCs) are clinically aggressive subtypes of breast cancer. TNBC is difficult to treat with targeted agents due to the lack of commonly targeted therapies within this subtype. Androgen receptor (AR) has been detected in 12-55% of TNBCs. AR stimulates breast tumor growth in the absence of estrogen receptor (ER), and it has become an emerging molecular target in TNBC treatment. Methods Ceritinib is a small molecule inhibitor of tyrosine kinase and it is used in the therapy of non-small lung cancer patients. Enzalutamide is a small molecule compound targeting the androgen receptor and it is used to treat prostate cancer. Combination therapy of these drugs were investigated using AR positive breast cancer mouse xenograft models. Also, combination treatment of ceritinib and paclitaxel investigated using AR(-) and AR low mouse xenograft and patient derived xenograft models. Results We screened 133 FDA approved drugs that have a therapeutic effect of AR(+) TNBC cells. From the screen, we identified two drugs, ceritinib and crizotinib. Since ceritinib has a well- defined role in androgen independent AR signaling pathways, we further investigated the effect of ceritinib. Ceritinib treatment inhibited RTK/ACK/AR pathway and other downstream pathways in AR(+) TNBC cells. The combination of ceritinib and enzalutamide showed a robust inhibitory effect on cell growth of AR(+) TNBC cells in vitro and in vivo. Interestingly Ceritinib inhibits FAK-YB-1 signaling pathway that leads to paclitaxel resistance in all types of TNBC cells. The combination of paclitaxel and ceritinib showed drastic inhibition of tumor growth compared to a single drug alone. Conclusions To improve the response of AR antagonist in AR positive TNBC, we designed a novel combinational strategy comprised of enzalutamide and ceritinib to treat AR(+) TNBC tumors through the dual blockade of androgen-dependent and androgen-independent AR signaling pathways. Furthermore, we introduced a novel therapeutic combination of ceritinib and paclitaxel for AR negative or AR-low TNBCs and this combination inhibited tumor growth to a great extent. All agents used in our study are FDA-approved, and thus the proposed combination therapy will likely be useful in the clinic.
引用
收藏
页数:16
相关论文
共 50 条
  • [31] Therapeutic targeting of ERβ in triple negative breast cancer
    Reese, Jordan M.
    Subramaniam, Malayannan
    Suman, Vera J.
    Wu, Xianglin
    Negron, Vivian
    Gingery, Anne
    Pitel, Kevin S.
    Shah, Sejal S.
    Cunliffe, Heather E.
    McCullough, Ann E.
    Pockaj, Barbara A.
    Spelsberg, Thomas C.
    Goetz, Matthew P.
    Ingle, James N.
    Hawse, John R.
    CANCER RESEARCH, 2015, 75
  • [32] Triple Negative Breast Cancer: Therapeutic and Prognostic Implications
    Brady-West, Doreen C.
    McGrowder, Donovan A.
    ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2011, 12 (08) : 2139 - 2143
  • [33] The therapeutic potential of melittin in triple negative breast cancer
    Hegde, Riya
    Hua, Claire
    Aguilar, Robert
    JOURNAL OF IMMUNOLOGY, 2024, 212 (01):
  • [34] YB1 is a novel therapeutic for the treatment of triple negative breast cancer tumors
    Wang, Wei
    El Khalki, Lamyae
    Zai, Neelum Yousaf
    Szpendyk, Justin
    Alkrekshi, Akram
    Su, Bin
    Sossey-Alaoui, Khalid
    CANCER RESEARCH, 2024, 84 (06)
  • [35] Unveiling Novel Therapeutic Drug Targets and Prognostic Markers of Triple Negative Breast Cancer
    Balkrishna, Acharya
    Mittal, Rashmi
    Arya, Vedpriya
    CURRENT CANCER DRUG TARGETS, 2021, 21 (11) : 907 - 918
  • [36] Investigation of novel therapeutic and diagnostic strategies for the management of triple-negative breast cancer
    Morrison, Chevaun Danielle
    Schlemann, William
    CANCER RESEARCH, 2013, 73
  • [37] Calcium Channel Blockers as Novel Therapeutic Agents for Triple-Negative Breast Cancer
    Lawler, Destiny
    Copeland, Robert L.
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2023, 385
  • [38] CDC20 is a novel therapeutic target in triple-negative breast cancer
    Sharma, Jayesh K.
    Alluri, Prasanna
    Udden, Nashir
    CANCER RESEARCH, 2020, 80 (16)
  • [39] SRC as a novel therapeutic target fot the treatment of triple negative breast cancer (TNBC)
    Walsh, S.
    Tryfonopoulos, D.
    Quinn, C.
    Flanagan, L.
    Pierce, A.
    McDermott, E. W.
    Evoy, D.
    O'Donovan, N.
    Crown, J.
    Duffy, M. J.
    BRITISH JOURNAL OF SURGERY, 2011, 98 : 25 - 26
  • [40] Targeted Therapeutic Strategies for Triple-Negative Breast Cancer
    Li, Ying
    Zhan, Zhijun
    Yin, Xuemin
    Fu, Shujun
    Deng, Xiyun
    FRONTIERS IN ONCOLOGY, 2021, 11