Potential Movement of CDK 4/6 Inhibitor from Cell Cycle Arrest to Immune Activation in Breast Cancer
Pamungkas Bagus Satriyo1,2*
1International Ph.D. Program in Medicine, College of Medicine, Taipei Medical University, Taipei City, Taiwan
2Doctoral Program of Medical Science and Health, Faculty of Medicine Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia
Submission: February 13, 2019: Published: February 27, 2019
*Corresponding Address: Pamungkas Bagus Satriyo, International Ph.D. Program in Medicine, College of Medicine, Taipei Medical University, Taipei City, Taiwan & Doctoral Program of Medical Science and Health, Faculty of Medicine Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia Canc
How to cite this article: Pamungkas Bagus Satriyo. Potential Movement of CDK 4/6 Inhibitor from Cell Cycle Arrest to Immune Activation in Breast Cancer. Canc Therapy & Oncol Int J. 2019; 13(1): 555855. DOI:10.19080/CTOIJ.2019.13.555855
Abstract
Three different CDK 4/6 inhibitor was approved in a short time during 2016-2017 by FDA to treat hormone receptor-positive (HR+), HER2 negative (-) advances breast cancer patients. Since the beginning of the preclinical study, palbociclib, ribociclib, and abemaciclib were markedly suppressed proliferations of HR+/HER2- cell lines but less effective to HER2+ and Triple Negative Breast Cancer. This suppression mechanism acts through the CKD4/6-Rb-E2F axis. In addition, recent studies found CDK 4/6 inhibitors activate the immune cells against tumor cell in HER2+ and TNBC subtypes. It also enhances breast cancer patients to immunotherapy. Here we provided short evidence of immune activation in breast cancer treated by CDK 4/6 inhibitor in alone or combinations. By understanding new mechanism CDK 4/6 inhibitor in immune activation, it increases the subtypes of breast cancer patients get benefit from CDK 4/6 inhibitor also improve the response to current immunotherapy.
Keywords: CDK 4/6 inhibitor; Breast cancer; Immune
Abbreviations: CDK 4/6: Cyclin Dependent Kinase 4/6; HR: Hormone Receptor; HER2: Human epidermal growth factor receptor 2; MMTV-rtTA/tetO-Her2: Reverse Tetracycline-Controlled Transactivator under control of the Mouse Mammary Tumor Virus promoter/ tetracycline (tet)-operator HER2
Introduction
Rapid advance movement of CDK 4/6 inhibitor from preclinical to the clinical trial becomes a new hope for advances (metastatic) breast cancer. The first CDK 4/6 inhibitor is palbociclib that approved for HR+/ HER2- advanced or metastatic breast cancer with disease progression after endocrine therapy. Palbociclib was being used in combination with fulvestrant [1]. Ribociclib was approved by FDA as the first line therapy to treat HR+/ HER2- advanced or metastatic breast cancer patients combined with letrozole [2]. Recently generation of CDK 4/6 inhibitor, Ribociclib was approved either alone or in combination with fulvestrant for advanced or metastatic HR+/ HER2- breast cancer after endocrine therapy failure [3].
Targeting the abnormal cell cycle of the tumor cells is the chief mechanism of CDK 4/6 inhibitor. In the activation of CDK4/6 through cycling D binding, the cyclin D-CDK4/6 complex phosphorylates the retinoblastoma (Rb) tumor suppressor protein. The phosphorylation of Rb protein releases its suppression effect to E2F transcription factor lead to activate the genes target and move the cells from G1 phase to S phase. In the present of CDK 4/6 inhibitor, phosphorylation of Rb protein was inhibited and suppresses E2F. In turn, it keeps the gene targets off [4–6]. Despite the cell cycle arrest mechanism as the main mechanism, there are emerging evidences that this drug has an important role in tumor microenvironment regulations in the breast cancer cells [5].
Tumor microenvironment consists of non-cellular and cellular components such as immune cells. Only targeting the cancer cells and ignoring the tumor microenvironment to eradicate the tumor is not enough since the relationship between both are support each other. Clinically, the tumor microenvironment such as infiltration of immune cells in the tumor site shows significant prognostic value of breast cancer patients. Tumor-infiltrating leucocyte studied most extensively in breast cancer. The TILs consist of T-cell, B-cell, monocyte, NK-cell, and cytotoxic T cell [7]. High TILs concentration in the Luminal-HER2 negative, HER2 positive and triple negative breast cancer (TNBC) subtypes of patients significantly associated with high pathologic complete responses (pCR) after neoadjuvant chemotherapy. Increases the TILs associated with longer overall survival of TNBC. By contrast, increasing in TILs has no association to overall survival in HER2 positive patients, even associate with shorter overall survival in luminal-HER2 negative subtypes [8]. This results in HER2 positive and luminal subtypes maybe caused by the existence of lymphocytes that suppresses the immune system and promotes tumor progression such as T-regulator cell, and myeloid-derived suppressor cell [9]. After success in melanoma and lung cancer patients, immunotherapy rapidly grows to treat the other solid cancer patients including breast cancer. After a low response of breast cancer patients to immunotherapy, recently good news came from TNBC patients’ study. Treatment atezolizumab to advanced TNBC with positive PD-L1 expression improve prolong free survival time compared to patients only got chemotherapy as standard treatment. In the middle of this good achievement still left a big question for the PD-L1 negative metastatic breast cancer patients (approximately 59.1%) [10].
Despite inducing G1 cell cycle arrest, growing evidences show CDK 4/6 inhibitor impressive effect on immune activation against breast cancer. Using breast cancer clinical samples, breast cancer cell line, and MMTV-rtTA/tetO-Her2 mice model, treatment abemaciclib inhibit tumor cell proliferation as well as activate the immune cells. First, this drug treatment induces dsRNA through increasing retroviral element endogenous expression. Next turn, it stimulates type III interferons and induces increasing tumor antigen presentation. In the other hand, these drugs also suppress the regulatory T cells proliferation but not the CD8+ or conventional CD4+ T cells. Further, both mechanisms enhance cytotoxic T cell eliminate the breast tumor cells [11]. Interestingly, in prostate cancer, Cyclin D-CDK4 axis regulates PDL-1 expression level through Cullin 3SPOP E3 ligase (Cul3SPOP). Cyclin D-CDK4 inhibition suppresses SPOP phosphorylation led to SPOP degradation by APC/CCdh1. This turn decreases PD-L1 ubiquitination and stabilizes its expression on the tumor cells. CDK 4/6 inhibitor treatment alone improve the survival rate compared to the control group in mouse tumor model. Moreover, combination CDK 4/6 inhibitor with anti-PD-1 immunotherapy significantly improve the survival rates compare to both drug-treated in alone [12]. Consistently, in the MMTV-rtTA/tetO-HER2 tumor mice showed similar results. Combination CDK 4/6 inhibitor (abemaciclib) and anti-PDL1therapy reduced tumor volume up to 70% at 13 days after initial treatment and stop growing at day 35 [11]. These findings open new hope to improve more breast cancer patients get benefit from immunotherapy through CDK 4/6 combination. This combination gives more chance for negative PD-L1 breast cancer patient to response the anti-PD-L1 immunotherapy.
At the beginning of CDK4/6 treatment on triple negative breast cancer subtypes, this drug showed little effect on suppressing cell proliferation. Recently, there growing evidences of chance using this drug to TNBC. In 2016, treated triplenegative breast cancer patient-derived xenograft mice with CDK 4/6 inhibitor could suppress the metastases process. Markedly, palbociclib significantly decreased distant metastases rates to liver (12.5% vs 75%), and lung (25% vs 75%) compare to control group (saline). This study also revealed the mechanism of metastases suppression happen through epithelialmesenchymal transition. CDK 4/6 inhibition suppresses DUB3 activation lead to destabilizing a key factor promoting EMT, SNAIL1 [13]. In another study, EMT in triple negative breast cancer has an important role in immune cell infiltration to the tumor sites and its activation. Tumors that arise from mesenchymal breast cancer cell lines show immune suppressive phenotype than tumor arising from epithelial cell lines. In mouse model injected with PyMT-Snail high cell lines arising tumors that have more regulatory T cells, M2 macrophages, PDL1, and low level of MHC-I as well as low activated CD8+ T cells [14]. Moreover, a combination between CDK 4/6 inhibitor and PI3Kα in syngeneic TNBC mouse model significantly increased cytotoxicity and activation of T cells in the tumor sites as well as suppressed the myeloid-derived suppressor cells populations [15].
Conclusion
In the success of immunotherapy against several solid tumors such as melanoma and lung cancer, there is a new hope of breast cancer patients get benefit through the same approach. However, the successful rate still remains low. Here we shortly provide evidences of CDK 4/6 inhibitor effect to immune cells in HER2 and triple negative breast cancer subtypes. By understanding the CDK 4/6 mechanism on immune cell activation, we hope there is a chance to increase the number of breast cancer subtypes get benefit from these drugs. Later, by combinations therapy, CDK 4/6 inhibitor could improve the response of breast cancer patients to current immunotherapy in the future.
References
- Walker AJ, Wedam S, Amiri-Kordestani L, Bloomquist E, Tang S, et al. (2016) FDA approval of palbociclib in combination with fulvestrant for the treatment of hormone receptor-positive, HER2-negative metastatic breast cancer. Clin Cancer Res 22(20): 4968–4972.
- Shah A, Erik Bloomquist, Shenghui Tang, Wentao Fu, Youwei Bi, et al. (2018) FDA approval: Ribociclib for the treatment of postmenopausal women with hormone receptor-positive, HER2-negative advanced or metastatic breast cancer. Clinical Cancer Research 24: 2999–3004.
- Matthew P. Goetz, Miguel Martin, Angelo Di Leo, Seock-Ah Im, Ahmad Awada, et al. (2018) Abstract CT040: MONARCH 3: Abemaciclib as initial therapy for patients with HR+, HER2- advanced breast cancer - Results from the preplanned final PFS analysis. Cancer Res 78(13): CT040-CT040.
- Goel S, DeCristo MJ, McAllister SS, Zhao JJ (2018) CDK4/6 Inhibition in Cancer: Beyond Cell Cycle Arrest. Trends Cell Biol 28(11): 911–925.
- Klein ME, Kovatcheva M, Davis LE, Tap WD, Koff A (2018) CDK4/6 Inhibitors: The Mechanism of Action May Not Be as Simple as Once Thought. Cancer Cell 34(1): 9–20.
- Pernas S, Tolaney SM, Winer EP, Goel S (2018) CDK4/6 inhibition in breast cancer: current practice and future directions. Ther Adv Med Oncol 10: 1–15.
- Melichar B, Študentova H, Kalábová H, Vitásková D, Čermáková P, et al. (2014) Predictive and Prognostic Significance of Tumor-infiltrating Lymphocytes in Patients with Breast Cancer Treated with Neoadjuvant Systemic Therapy. Anticancer Res 34(3): 1115–1125
- Denkert C, Gunter Von Minckwitz, Silvia Darb Esfahani, Bianca Lederer, Barbara I Heppner, et al. (2018) Tumour-infiltrating lymphocytes and prognosis in different subtypes of breast cancer: a pooled analysis of 3771 patients treated with neoadjuvant therapy. Lancet Oncol 19(1): 40–50.
- Nakasone ES, Hurvitz SA, McCann KE (2018) Harnessing the immune system in the battle against breast cancer. Drugs Context 7: 212520.
- Peter Schmid, Sylvia Adams, Hope S Rugo, Andreas Schneeweiss, Carlos H Barrios, et al. (2018) Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer. N Engl J Med 379: 2108-2121.
- Goel S, DeCristo MJ, Watt AC, BrinJones H, Sceneay J, et al. (2017) CDK4/6 inhibition triggers anti-tumour immunity. Nature, 548(7668): 471–475.
- Zhang J, Bu X, Wang H, Zhu Y, Geng Y, et al. (2018) Cyclin D-CDK4 kinase destabilizes PD-L1 via cullin 3-SPOP to control cancer immune surveillance. Nature 553(7686): 91–95.
- Liu T, Yu J, Deng M, Yin Y, Zhang H, et al. (2017) CDK4/6-dependent activation of DUB3 regulates cancer metastasis through SNAIL1. Nat Commun 8: 13923.
- Dongre A, Rashidian M, Reinhardt F, Bagnato A, Keckesova Z, et al. (2017) Epithelial-to-mesenchymal transition contributes to immunosuppression in breast carcinomas. Cancer Res 77(15): 3982– 3989.
- Teo ZL, Versaci S, Dushyanthen S, Caramia F, Savas P, et al. (2017) Combined CDK4/6 and PI3Kα inhibition is synergistic and immunogenic in triple-negative breast cancer. Cancer Res 77(22): 6340–6352.