Deciphering treatment resistance in metastatic colorectal cancer: roles of drug transports, EGFR mutations, and HGF/c-MET signaling

被引:8
作者
Albadari, Najah [1 ]
Xie, Yang [1 ]
Li, Wei [1 ]
机构
[1] Univ Tennessee, Hlth Sci Ctr, Coll Pharm, Memphis, TN USA
关键词
metastatic colorectal cancer; resistance; anti-EGFR; anti-MET; ABC drug transporters; tyrosine kinase inhibitors; GROWTH-FACTOR RECEPTOR; TIVANTINIB ARQ 197; BINDING CASSETTE SUBFAMILY; WILD-TYPE KRAS; MULTIDRUG-RESISTANCE; COLON-CANCER; C-MET; PHASE-II; CETUXIMAB RESISTANCE; THYMIDYLATE SYNTHASE;
D O I
10.3389/fphar.2023.1340401
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In 2023, colorectal cancer (CRC) is the third most diagnosed malignancy and the third leading cause of cancer death worldwide. At the time of the initial visit, 20% of patients diagnosed with CRC have metastatic CRC (mCRC), and another 25% who present with localized disease will later develop metastases. Despite the improvement in response rates with various modulation strategies such as chemotherapy combined with targeted therapy, radiotherapy, and immunotherapy, the prognosis of mCRC is poor, with a 5-year survival rate of 14%, and the primary reason for treatment failure is believed to be the development of resistance to therapies. Herein, we provide an overview of the main mechanisms of resistance in mCRC and specifically highlight the role of drug transports, EGFR, and HGF/c-MET signaling pathway in mediating mCRC resistance, as well as discuss recent therapeutic approaches to reverse resistance caused by drug transports and resistance to anti-EGFR blockade caused by mutations in EGFR and alteration in HGF/c-MET signaling pathway.
引用
收藏
页数:24
相关论文
共 304 条
[31]   The Role of the Tumor Microenvironment and Treatment Strategies in Colorectal Cancer [J].
Chen, Yaping ;
Zheng, Xiao ;
Wu, Changping .
FRONTIERS IN IMMUNOLOGY, 2021, 12
[32]   Metastatic colorectal cancer cells maintain the TGFβ program and use TGFBI to fuel angiogenesis [J].
Chiavarina, Barbara ;
Costanza, Brunella ;
Ronca, Roberto ;
Blomme, Arnaud ;
Rezzola, Sara ;
Chiodelli, Paola ;
Giguelay, Ambre ;
Belthier, Guillame ;
Doumont, Gilles ;
Van Simaeys, Gaetan ;
Lacroix, Simon ;
Yokobori, Takehiko ;
Erkhem-Ochir, Bilguun ;
Balaguer, Patrick ;
Cavailles, Vincent ;
Fabbrizio, Eric ;
Di Valentin, Emmanuel ;
Gofflot, Stephanie ;
Detry, Olivier ;
Jerusalem, Guy ;
Goldman, Serge ;
Delvenne, Philippe ;
Bellahcene, Akeila ;
Pannequin, Julie ;
Castronovo, Vincent ;
Turtoi, Andrei .
THERANOSTICS, 2021, 11 (04) :1626-1640
[33]   Drug development of MET inhibitors: targeting oncogene addiction and expedience [J].
Comoglio, Paolo M. ;
Giordano, Silvia ;
Trusolino, Livio .
NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (06) :504-516
[34]   EGFR-Mediated Reactivation of MAPK Signaling Contributes to Insensitivity of BRAF-Mutant Colorectal Cancers to RAF Inhibition with Vemurafenib [J].
Corcoran, Ryan B. ;
Ebi, Hiromichi ;
Turke, Alexa B. ;
Coffee, Erin M. ;
Nishino, Michiya ;
Cogdill, Alexandria P. ;
Brown, Ronald D. ;
Della Pelle, Patricia ;
Dias-Santagata, Dora ;
Hung, Kenneth E. ;
Flaherty, Keith T. ;
Piris, Adriano ;
Wargo, Jennifer A. ;
Settleman, Jeffrey ;
Mino-Kenudson, Mari ;
Engelman, Jeffrey A. .
CANCER DISCOVERY, 2012, 2 (03) :227-235
[35]   Beyond PTEN mutations: the PI3K pathway as an integrator of multiple inputs during tumorigenesis [J].
Cully, M ;
You, H ;
Levine, AJ ;
Mak, TW .
NATURE REVIEWS CANCER, 2006, 6 (03) :184-192
[36]   Enhancing the Radiation Response in KRAS Mutant Colorectal Cancers Using the c-Met Inhibitor Crizotinib [J].
Cuneo, Kyle C. ;
Mehta, Ranjit K. ;
Kurapati, Himabindu ;
Thomas, Dafydd G. ;
Lawrence, Theodore S. ;
Nyati, Mukesh K. .
TRANSLATIONAL ONCOLOGY, 2019, 12 (02) :209-216
[37]   Gene Expression Markers of Efficacy and Resistance to Cetuximab Treatment in Metastatic Colorectal Cancer: Results from CALGB 80203 (Alliance) [J].
Cushman, Stephanie M. ;
Jiang, Chen ;
Hatch, Ace J. ;
Shterev, Ivo ;
Sibley, Alexander B. ;
Niedzwiecki, Donna ;
Venook, Alan P. ;
Owzar, Kouros ;
Hurwitz, Herbert I. ;
Nixon, Andrew B. .
CLINICAL CANCER RESEARCH, 2015, 21 (05) :1078-1086
[38]   DNA topoisomerase-targeting chemotherapeutics: what's new? [J].
Cuya, Selma M. ;
Bjornsti, Mary-Ann ;
van Waardenburg, Robert C. A. M. .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2017, 80 (01) :1-14
[39]   Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2 [J].
Dai, Chun-ling ;
Tiwari, Amit K. ;
Wu, Chung-Pu ;
Su, Xiao-dong ;
Wang, Si-Rong ;
Liu, Dong-geng ;
Ashby, Charles R., Jr. ;
Huang, Yan ;
Robey, Robert W. ;
Liang, Yong-ju ;
Chen, Li-ming ;
Shi, Cheng-Jun ;
Ambudkar, Suresh V. ;
Chen, Zhe-Sheng ;
Fu, Li-wu .
CANCER RESEARCH, 2008, 68 (19) :7905-7914
[40]   Individualization of Irinotecan Treatment: A Review of Pharmacokinetics, Pharmacodynamics, and Pharmacogenetics [J].
de Man, Femke M. ;
Goey, Andrew K. L. ;
van Schaik, Ron H. N. ;
Mathijssen, Ron H. J. ;
Bins, Sander .
CLINICAL PHARMACOKINETICS, 2018, 57 (10) :1229-1254