Anti-Cancer Effects of CDK4/6 Inhibitor LEE011 and Chemotherapy Drugs on Lymphocytic Leukemia L1210 Cells

被引:0
|
作者
Lin, Yu-cheng [1 ]
Lin, Yuan-ho [1 ,2 ]
Chang, Yu [3 ,4 ]
Su, Yu-chieh [5 ,6 ]
Hsieh, Wen-chuan [7 ]
Chen, Wen-hui [6 ,8 ]
Lee, Hui-ming [1 ,9 ,10 ]
机构
[1] I Shou Univ, E Da Canc Hosp, Dept Chinese Med, Kaohsiung, Taiwan
[2] I Shou Univ, Sch Chinese Med Postbaccalaureate, Coll Med, Kaohsiung, Taiwan
[3] I Shou Univ, E Da Hosp, Dept Obstet & Gynecol, Kaohsiung, Taiwan
[4] I Shou Univ, Coll Med, Sch Med Int Students, Kaohsiung, Taiwan
[5] I Shou Univ, E Da Hosp, Dept Internal Med, Div Hematol Oncol, Kaohsiung, Taiwan
[6] I Shou Univ, Coll Med, Sch Med, Kaohsiung, Taiwan
[7] I Shou Univ, Coll Med Sci & Technol, Dept Biol Sci & Technol, Kaohsiung, Taiwan
[8] I Shou Univ, E Da Hosp, Dept Dent, Kaohsiung, Taiwan
[9] I Shou Univ, E Da Canc Hosp, Dept Surg, Div Gen Surg, 1 Yida Rd, Kaohsiung 82445, Taiwan
[10] I Shou Univ, Coll Med, Sch Chinese Med Post Baccalaureate, Kaohsiung, Taiwan
关键词
Cell cycle; CDK4/6; inhibitor; LEE011; bendamustine; hydroxyurea; GROWTH;
D O I
10.21873/anticanres.16907
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Chronic lymphocytic leukemia is a slowly -progressing disease in which symptoms often do not manifest until years after disease onset. In advanced stages, infection and bleeding are common. Past studies have shown that the interaction between CDK4/6 inhibitors and chemotherapy drugs can enhance the anti -tumor efficacy of drugs and limit toxicity. Therefore, in this study, the treatment effects of combining the CDK4/6 inhibitor LEE011 with chemotherapy drugs bendamustine or hydroxyurea were investigated in vitro. Materials and Methods: The mouse lymphocytic leukemia cell line L1210 was treated with LEE011 combined with hydroxyurea or bendamustine. Western blot and flow cytometry were performed to elucidate the mechanisms behind tumor suppression. Results: LEE011 combined with hydroxyurea or bendamustine significantly inhibited proliferation of L1210 cell lines in a concentrationand time -dependent manner as well as increased the arrest of cells in G1 and S phases. The combination of LEE011 with hydroxyurea also reduced the phosphorylation of Rb while increased the expression of total Rb protein. Furthermore, reduced expression of GPX4, which is a key protein in ferroptosis, indicates that the tumor suppression effects of this drug combination could involve ferroptosis. Conclusion: CDK4/6 inhibitor LEE011 treatment alone may not be a suitable treatment option for lymphocytic leukemia; however, our findings in vitro support the combination of LEE011 with chemotherapy drugs to enhance anti -tumor activity in lymphocytic leukemia.
引用
收藏
页码:1121 / 1130
页数:10
相关论文
共 41 条
  • [21] Synergistic anti-cancer activity of the CDK4/6 inhibitor PD-0332991 in combination with 5-fluorouracil-based chemotherapy in human colon cancer cells
    Pishvaian, Michael J.
    Yang, Shaoxian
    El Zouhairi, Majed
    Wu, Christina S.
    Mishra, Lopa
    Avantaggiati, Maria-Laura
    CANCER RESEARCH, 2010, 70
  • [22] Synergistic anti-cancer activity of the CDK4/6 inhibitor PD-0332991 in combination with 5-fluorouracil-based chemotherapy in human colon cancer cells
    Pishvaian, Michael J.
    Yang, Shaoxian
    El Zouhairi, Majed
    Wu, Christina S.
    Mishra, Lopa
    Avantaggiati, Maria-Laura
    CANCER RESEARCH, 2010, 70
  • [23] A phase 1b/2 study of ribociclib (LEE011; CDK4/6 inhibitor) in combination with binimetinib (MEK162; MEK inhibitor) in patients with NRAS-mutant melanoma
    Van Herpen, C.
    Postow, M. A.
    Carlino, M. S.
    Kalkavan, H.
    Weise, A.
    Amaria, R. N.
    De Vos, F.
    Carvajal, R. D.
    Matano, A.
    Bhansali, S.
    Lam, L.
    Yerramilli-Rao, P.
    Sosman, J. A.
    EUROPEAN JOURNAL OF CANCER, 2015, 51 : S663 - S663
  • [24] Novel translational pharmacology approaches on dose reduction and alternative scheduling for the combination of JAK inhibitor, ruxolitinib, PIM inhibitor, LGH447, and CDK4/6 inhibitor, LEE011 in a preclinical model of myeloproliferative neoplasia
    Pinzon-Ortiz, Maria
    Rong, Xianhui
    Vanasse, Gary
    Cao, Z. Alexander
    CANCER RESEARCH, 2015, 75
  • [25] Gilteritinib Enhances Anti-Tumor Efficacy of CDK4/6 Inhibitor, Abemaciclib in Lung Cancer Cells
    Sun, Chao-Yue
    Talukder, Milton
    Cao, Di
    Chen, Cun-Wu
    FRONTIERS IN PHARMACOLOGY, 2022, 13
  • [26] POTENTIATION OF THE CYTO-TOXIC ACTIVITY OF ANTI-CANCER DRUGS AGAINST CULTURED L1210 CELLS BY BACILLUS-THURINGIENSIS SUBSP ISRAELENSIS TOXIN
    YOKOYAMA, Y
    OHMORI, I
    KOHDA, K
    KAWAZOE, Y
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1988, 36 (11) : 4499 - 4504
  • [27] Modulation of SIRT3 expression through CDK4/6 enhances the anti-cancer effect of sorafenib in hepatocellular carcinoma cells
    Jo, Hanhee
    Park, Yusun
    Kim, Taehun
    Kim, Jisu
    Lee, Jong Sook
    Kim, Seon Yoo
    Chung, Jee-in
    Ko, Hae Yong
    Pyun, Jae-Chul
    Kim, Kyung Sik
    Lee, Misu
    Yun, Mijin
    BMC CANCER, 2020, 20 (01)
  • [28] Modulation of SIRT3 expression through CDK4/6 enhances the anti-cancer effect of sorafenib in hepatocellular carcinoma cells
    Hanhee Jo
    Yusun Park
    Taehun Kim
    Jisu Kim
    Jong Sook Lee
    Seon Yoo Kim
    Jee-in Chung
    Hae yong Ko
    Jae-Chul Pyun
    Kyung Sik Kim
    Misu Lee
    Mijin Yun
    BMC Cancer, 20
  • [29] NEW ANTI-CANCER PRINCIPLE ISOLATED FROM GYMNOSPORIA-ROTHIANA LAWS, AND ITS USE IN ATTAINING CURES IN L1210 LEUKEMIA IN COMBINATION WITH (S) PHASE SENSITIVE DRUGS
    ALATE, AD
    KHANDALEKAR, DD
    AMONKAR, AJ
    ADWANKAR, MK
    SAHASRABUDHE, MB
    BIOMEDICINE, 1978, 28 (05): : 270 - 273
  • [30] NOVEL CDK4/6 INHIBITOR - WXJ-8-EXERTS ANTI-EFFECTS THROUGH CELL CYCLE IN BREAST CANCER
    Ji, Jing
    Han, Jin-Qing
    Hou, Xiao
    Zhang, Zhen
    Li, Guan-Chun
    Zuo, Ling-Yi
    Zhou, Jiao-Jiao
    Wang, Xiu-Jun
    Ma, Shao-Jie
    Liu, Bin
    ACTA POLONIAE PHARMACEUTICA, 2023, 80 (05): : 763 - 773