Combination treatment of bortezomib and epirubicin increases the expression of TNFRSF10 A/B, and induces TRAIL-mediated cell death in colorectal cancer cells

被引:5
|
作者
Caldiran, Feyzanur [1 ]
Berkel, Caglar [1 ]
Yilmaz, Esra [1 ]
Kucuk, Burak [1 ]
Cacan, Aslihan Hatun [2 ]
Citli, Senol [3 ]
Canpolat, Emel [1 ]
Cacan, Ercan [1 ,4 ]
机构
[1] Tokat Gaziosmanpasa Univ, Fac Sci & Art, Dept Mol Biol & Genet, Tokat, Turkiye
[2] Tokat Gaziosmanpasa Univ, Dept Med Serv & Tech, Tokat, Turkiye
[3] Recep Tayyip Erdogan Univ, Fac Med, Dept Med Genet, Rize, Turkiye
[4] Tokat Gaziosmanpasa Univ, Fac Sci & Art, Dept Mol Biol & Genet, TR-60250 Tokat, Turkiye
关键词
TRAIL-DR; TNFRSF10A; TNFRSF10B; Bortezomib; Epirubicin; Colorectal cancer; INDUCED APOPTOSIS; PROTEASOME INHIBITOR; CISPLATIN; SURVIVAL;
D O I
10.1016/j.bbrc.2023.06.015
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
Colorectal cancer is one of the most common cancers worldwide, affecting the colon and rectum. A major problem in the treatment of colorectal cancer is acquired chemoresistance, including resistance against death receptor-induced apoptosis. Therefore, investigating new biomarkers for the treatment of the disease and sensitization strategies against TRAIL might be of high clinical importance. TNFRSF10A/B are known as death receptors for TRAIL-induced apoptotic cell death. In this study, we used multiple bioinformatic tools and experimental analyses to investigate the role of TRAIL receptors TNFRSF10A and TNFRSF10B in colorectal cancer. We also identified the potential effect of bortezomib and epirubicin in the induction of TRAIL-mediated apoptotic cell death. Here, we showed that TNFRSF10 A/B expressions are upregulated in various tumor types, including COAD, and its high expression is decreased with the different clinicopathological parameters in COAD. We also found an association between TNFRSF10 A/B expression and tumor molecular subtypes. We further detected the association between the expression of TNFRSF10 A/B and immune cell tumor infiltration, including B cells, CD8 thorn T cells, neutrophils and dendritic cells. In addition, we showed that combining bortezomib and epirubicin treatment leads to the upregulation of TNFRSF10 A/B in colorectal cancer cells in vitro. The increase in the expression of death receptors was correlated with higher active caspase-3 levels following the incubation of cells with recombinant TRAIL protein, which is a ligand for TNFRSF10 A/B receptors. Our results suggest that TNFRSF10 A/B may be a marker to differentiate tumor molecular subtypes in colorectal cancer. The expression of TNFRSF10 A/B may be associated with the recruitment of immune cells into tumors and the development of tumor suppression. The combination of bortezomib and epirubicin treatment might sensitize colorectal cancer cells to TRAIL-induced apoptosis via the upregulation of death receptor. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
相关论文
共 50 条
  • [1] The combination of TRAIL treatment and cancer cell selective expression of TRAIL-death receptor DR4 induces cell death in TRAIL-resistant cancer cells
    Choi, E
    Kim, Y
    Kim, K
    YONSEI MEDICAL JOURNAL, 2006, 47 (01) : 55 - 62
  • [2] A small molecule Smac mimic potentiates TRAIL-mediated cell death of ovarian cancer cells
    Petrucci, Eleonora
    Pasquini, Luca
    Petronelli, Alessia
    Saulle, Ernestina
    Mariani, Gualtiero
    Riccioni, Roberta
    Biffoni, Mauro
    Ferretti, Gianlulgi
    Benedetti-Panici, Pieluigi
    Cognetti, Francesco
    Scambia, Giovanni
    Humphreys, Robin
    Peschle, Cesare
    Testa, Ugo
    GYNECOLOGIC ONCOLOGY, 2007, 105 (02) : 481 - 492
  • [3] Targeted knockdown of death-associated protein kinase expression induces TRAIL-mediated apoptosis in human endometrial adenocarcinoma cells
    Bai, Tao
    Tanaka, Tetsuji
    Yukawa, Kazunori
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 37 (01) : 203 - 210
  • [4] MK-2206 induces cell cycle arrest and apoptosis in HepG2 cells and sensitizes TRAIL-mediated cell death
    Peng Jiao
    Yun-Sheng Zhou
    Juan-Xia Yang
    Ya-Li Zhao
    Qiang-Qiang Liu
    Chuang Yuan
    Feng-Ze Wang
    Molecular and Cellular Biochemistry, 2013, 382 : 217 - 224
  • [5] MK-2206 induces cell cycle arrest and apoptosis in HepG2 cells and sensitizes TRAIL-mediated cell death
    Jiao, Peng
    Zhou, Yun-Sheng
    Yang, Juan-Xia
    Zhao, Ya-Li
    Liu, Qiang-Qiang
    Yuan, Chuang
    Wang, Feng-Ze
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2013, 382 (1-2) : 217 - 224
  • [6] Mechanistic analysis of B16F10 melanoma cell death induced by treatment with recombinant TRAIL and bortezomib
    Ryu, S.
    Moon, A.
    Youn, C.
    Howland, A.
    Armstrong, C.
    Song, P.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2018, 138 (05) : S200 - S200
  • [7] Death Receptor 5 (TNFRSF10B) Is Upregulated and TRAIL Resistance Is Reversed in Hypoxia and Normoxia in Colorectal Cancer Cell Lines after Treatment with Skyrin, the Active Metabolite of Hypericum spp.
    Babincak, Marian
    Jendzelovsky, Rastislav
    Kosuth, Jan
    Majernik, Martin
    Vargova, Jana
    Mikulasek, Kamil
    Zdrahal, Zbynek
    Fedorocko, Peter
    CANCERS, 2021, 13 (07)
  • [8] Sodium Butyrate Inhibits the Expression of Thymidylate Synthase and Induces Cell Death in Colorectal Cancer Cells
    Kim, Nayeon
    Yang, Changwon
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (03)
  • [9] Piperlongumine induces cell death through ROS-mediated CHOP activation and potentiates TRAIL-induced cell death in breast cancer cells
    Jin, Hyeon-Ok
    Lee, Yun-Han
    Park, Jin-Ah
    Lee, Ha-Na
    Kim, Jin-Hee
    Kim, Ji-Young
    Kim, BoRa
    Hong, Sung-Eun
    Kim, Hyun-Ah
    Kim, Eun-Kyu
    Noh, Woo Chul
    Kim, Jong-Il
    Chang, Yoon Hwan
    Hong, Seok-Il
    Hong, Young-Jun
    Park, In-Chul
    Lee, Jin Kyung
    JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2014, 140 (12) : 2039 - 2046
  • [10] Piperlongumine induces cell death through ROS-mediated CHOP activation and potentiates TRAIL-induced cell death in breast cancer cells
    Hyeon-Ok Jin
    Yun-Han Lee
    Jin-Ah Park
    Ha-Na Lee
    Jin-Hee Kim
    Ji-Young Kim
    BoRa Kim
    Sung-Eun Hong
    Hyun-Ah Kim
    Eun-Kyu Kim
    Woo Chul Noh
    Jong-Il Kim
    Yoon Hwan Chang
    Seok-Il Hong
    Young-Jun Hong
    In-Chul Park
    Jin Kyung Lee
    Journal of Cancer Research and Clinical Oncology, 2014, 140 : 2039 - 2046