Interplay between Signaling Pathways and Tumor Microenvironment Components: A Paradoxical Role in Colorectal Cancer

被引:21
作者
Ben Hamouda, Sonia [1 ]
Essafi-Benkhadir, Khadija [1 ]
机构
[1] Univ Tunis El Manar, Inst Pasteur Tunis, Lab Epidemiol Mol & Pathol Expt, LR16IPT04, Tunis 1002, Tunisia
关键词
colorectal cancer; tumor microenvironment; signaling pathways; effectors; dual function; NF-KAPPA-B; GROWTH-FACTOR-BETA; PLASMACYTOID DENDRITIC CELLS; REGULATORY T-CELLS; WNT/BETA-CATENIN PATHWAY; MHC CLASS-I; COLON-CANCER; TGF-BETA; SUPPRESSOR-CELLS; OVARIAN-CANCER;
D O I
10.3390/ijms24065600
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
The study of the tumor microenvironment (TME) has become an important part of colorectal cancer (CRC) research. Indeed, it is now accepted that the invasive character of a primary CRC is determined not only by the genotype of the tumor cells, but also by their interactions with the extracellular environment, which thereby orchestrates the development of the tumor. In fact, the TME cells are a double-edged sword as they play both pro- and anti-tumor roles. The interaction of the tumor-infiltrating cells (TIC) with the cancer cells induces the polarization of the TIC, exhibiting an antagonist phenotype. This polarization is controlled by a plethora of interconnected pro- and anti-oncogenic signaling pathways. The complexity of this interaction and the dual function of these different actors contribute to the failure of CRC control. Thus, a better understanding of such mechanisms is of great interest and provides new opportunities for the development of personalized and efficient therapies for CRC. In this review, we summarize the signaling pathways linked to CRC and their implication in the development or inhibition of the tumor initiation and progression. In the second part, we enlist the major components of the TME and discuss the complexity of their cells functions.
引用
收藏
页数:34
相关论文
共 237 条
[1]   Treg-cell depletion promotes chemokine production and accumulation of CXCR3+ conventional T cells in intestinal tumors [J].
Akeus, Paulina ;
Langenes, Veronica ;
Kristensen, Jonas ;
von Mentzer, Astrid ;
Sparwasser, Tim ;
Raghavan, Sukanya ;
Quiding-Jarbrink, Marianne .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2015, 45 (06) :1654-1666
[2]   Targeting the TGFβ signalling pathway in disease [J].
Akhurst, Rosemary J. ;
Hata, Akiko .
NATURE REVIEWS DRUG DISCOVERY, 2012, 11 (10) :790-811
[3]   Fibroblasts in the Tumor Microenvironment: Shield or Spear? [J].
Alkasalias, Twana ;
Moyano-Galceran, Lidia ;
Arsenian-Henriksson, Marie ;
Lehti, Kaisa .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (05)
[4]   Understanding cell-cell communication and signaling in the colorectal cancer microenvironment [J].
AlMusawi, Shaikha ;
Ahmed, Mehreen ;
Nateri, Abdolrahman S. .
CLINICAL AND TRANSLATIONAL MEDICINE, 2021, 11 (02)
[5]   Notch signaling: simplicity in design, versatility in function [J].
Andersson, Emma R. ;
Sandberg, Rickard ;
Lendahl, Urban .
DEVELOPMENT, 2011, 138 (17) :3593-3612
[6]  
[Anonymous], Global Cancer Observatory
[7]   Interplay between MAPK/ERK signaling pathway and MicroRNAs: A crucial mechanism regulating cancer cell metabolism and tumor progression [J].
Asl, Elmira Roshani ;
Amini, Mohammad ;
Najafi, Souzan ;
Mansoori, Behzad ;
Mokhtarzadeh, Ahad ;
Mohammadi, Ali ;
Lotfinejad, Parisa ;
Bagheri, Mehdi ;
Shirjang, Solmaz ;
Lotfi, Ziba ;
Rasmi, Yousef ;
Baradaran, Behzad .
LIFE SCIENCES, 2021, 278
[8]   Cancer-associated fibroblasts as another polarized cell type of the tumor microenvironment [J].
Augsten, Martin .
FRONTIERS IN ONCOLOGY, 2014, 4
[9]   STAT3 in cancer: A double edged sword [J].
Avalle, Lidia ;
Camporeale, Annalisa ;
Camperi, Andrea ;
Poli, Valeria .
CYTOKINE, 2017, 98 :42-50
[10]   FGF-1/-3/FGFR4 signaling in cancer-associated fibroblasts promotes tumor progression in colon cancer through Erk and MMP-7 [J].
Bai, Yu-Pan ;
Shang, Kun ;
Chen, Huan ;
Ding, Fei ;
Wang, Zhen ;
Liang, Chen ;
Xu, Ye ;
Sun, Meng-Hong ;
Li, Ying-yi .
CANCER SCIENCE, 2015, 106 (10) :1278-1287