The footprint of kynurenine pathway in every cancer: a new target for chemotherapy

被引:73
作者
Ala, Moein [1 ]
机构
[1] Univ Tehran Med Sci, Sch Med, Tehran, Iran
关键词
Kynurenine pathway; Cancer; IDO; Indoximod; Immune system; AHR; ARYL-HYDROCARBON RECEPTOR; INDOLEAMINE 2,3-DIOXYGENASE EXPRESSION; ACUTE MYELOID-LEUKEMIA; REGULATORY T-CELLS; PROMOTES GENOMIC INSTABILITY; IDO1; INHIBITOR; BREAST-CANCER; COLORECTAL-CANCER; TUMOR-GROWTH; DENDRITIC CELLS;
D O I
10.1016/j.ejphar.2021.173921
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Treatment of cancers has always been a challenge for physicians. Typically, several groups of anti-cancer medications are needed for effective management of an invasive and metastatic cancer. Recently, therapeutic potentiation of immune system markedly improved treatment of cancers. Kynurenine pathway has an interwoven correlation with immune system. Kynurenine promotes T Reg (regulatory) differentiation, which leads to increased production of anti-inflammatory cytokines and suppression of cytotoxic activity of T cells. Overactivation of kynurenine pathway in cancers provides an immunologically susceptible microenvironment for mutant cells to survive and invade surrounding tissues. Interestingly, kynurenine pathway vigorously interacts with other molecular pathways involved in tumorigenesis. For instance, kynurenine pathway interacts with phospoinosisitide-3 kinase (PI3K), extracellular signal-regulated kinase (ERK), Wnt/beta-catenin, P53, bridging integrator 1 (BIN-1), cyclooxygenase 2 (COX-2), cyclin-dependent kinase (CDK) and collagen type XII a1 chain (COL12A1). Overactivation of kynurenine pathway, particularly overactivation of indoleamine 2,3-dioxygenase (IDO) predicts poor prognosis of several cancers such as gastrointestinal cancers, gynecological cancers, hematologic malignancies, breast cancer, lung cancer, glioma, melanoma, prostate cancer and pancreatic cancer. Furthermore, kynurenine increases the invasion, metastasis and chemoresistance of cancer cells. Recently, IDO inhibitors entered clinical trials and successfully passed their safety tests and showed promising therapeutic efficacy for cancers such as melanoma, brain cancer, renal cell carcinoma, prostate cancer and pancreatic cancer. However, a phase III trial of epacadostat, an IDO inhibitor, could not increase the efficacy of treatment with pembrolizumab for melanoma. In this review the expanding knowledge towards kynurenine pathway and its application in each cancer is discussed separately.
引用
收藏
页数:15
相关论文
共 237 条
[1]   Prognostic effect of epithelial and stromal lymphocyte infiltration in non-small cell lung cancer [J].
Al-Shibli, Khalid I. ;
Donnem, Tom ;
Al-Saad, Samer ;
Persson, Magnus ;
Bremnes, Roy M. ;
Busund, Lill-Tove .
CLINICAL CANCER RESEARCH, 2008, 14 (16) :5220-5227
[2]   1-Methyl-D-tryptophan Reduces Tumor CD133+ cells, Wnt/β-catenin and NF-κβp65 while Enhances Lymphocytes NF-κβ2, STAT3, and STAT4 Pathways in Murine Pancreatic Adenocarcinoma [J].
Alahdal, Murad ;
Xing, Yun ;
Tang, Tingting ;
Liang, Jin .
SCIENTIFIC REPORTS, 2018, 8
[3]  
Amobi-McCloud A.E, 2020, INDOLEAMINE 2 3 DIOX
[4]   Indoleamine 2,3-dioxygenase expression and overall survival in patients diagnosed with breast cancer in Pakistan [J].
Asghar, Kashif ;
Loya, Asif ;
Rana, Iftikhar Ali ;
Tahseen, Muhammad ;
Ishaq, Muhammad ;
Farooq, Asim ;
Abu Bakar, Muhammad ;
Masood, Iqra .
CANCER MANAGEMENT AND RESEARCH, 2019, 11 :475-481
[5]   Indoleamine 2,3-dioxygenase expression and activity in patients with hepatitis C virus-induced liver cirrhosis [J].
Asghar, Kashif ;
Ashiq, M. Taimour ;
Zulfiqar, Bilal ;
Mahroo, Amnah ;
Nasir, Kaenat ;
Murad, Sheeba .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2015, 9 (03) :901-904
[6]  
Badawy AAB, 2017, INT J TRYPTOPHAN RES, V10, DOI 10.1177/1178646917691938
[7]   Imatinib potentiates antitumor T cell responses in gastrointestinal stromal tumor through the inhibition of Ido [J].
Balachandran, Vinod P. ;
Cavnar, Michael J. ;
Zeng, Shan ;
Bamboat, Zubin M. ;
Ocuin, Lee M. ;
Obaid, Hebroon ;
Sorenson, Eric C. ;
Popow, Rachel ;
Ariyan, Charlotte ;
Rossi, Ferdinand ;
Besmer, Peter ;
Guo, Tianhua ;
Antonescu, Cristina R. ;
Taguchi, Takahiro ;
Yuan, Jianda ;
Wolchok, Jedd D. ;
Allison, James P. ;
DeMatteo, Ronald P. .
NATURE MEDICINE, 2011, 17 (09) :1094-U99
[8]   Expression of Indoleamine 2,3-Dioxygenase Induced by IFn-γ and TnF-α as Potential Biomarker of Prostate Cancer Progression [J].
Banzola, Irina ;
Mengus, Chantal ;
Wyler, Stephen ;
Hudolin, Tvrko ;
Manzella, Gabriele ;
Chiarugi, Alberto ;
Boldorini, Renzo ;
Sais, Giovanni ;
Schmidli, Tobias S. ;
Chiffi, Gabriele ;
Bachmann, Alexander ;
Sulser, Tullio ;
Spagnoli, Giulio C. ;
Provenzano, Maurizio .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[9]   First-in-Human Phase I Study of the Oral Inhibitor of Indoleamine 2,3-Dioxygenase-1 Epacadostat (INCB024360) in Patients with Advanced Solid Malignancies [J].
Beatty, Gregory L. ;
O'Dwyer, Peter J. ;
Clark, Jason ;
Shi, Jack G. ;
Bowman, Kevin J. ;
Scherle, Peggy A. ;
Newton, Robert C. ;
Schaub, Richard ;
Maleski, Janet ;
Leopold, Lance ;
Gajewski, Thomas F. .
CLINICAL CANCER RESEARCH, 2017, 23 (13) :3269-3276
[10]   The aryl hydrocarbon receptor (AhR) mediates resistance to apoptosis induced in breast cancer cells [J].
Bekki, Kanae ;
Vogel, Helena ;
Li, Wen ;
Ito, Tomohiro ;
Sweeney, Colleen ;
Haarmann-Stemmann, Thomas ;
Matsumura, Fumio ;
Vogel, Christoph F. A. .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2015, 120 :5-13