Cell death in tumor microenvironment: an insight for exploiting novel therapeutic approaches

被引:7
作者
Wang, Wenxin [1 ,2 ,3 ]
Li, Tong [1 ,2 ,3 ]
Wu, Kui [1 ,2 ,3 ]
机构
[1] BGI Genom, Shenzhen 518083, Peoples R China
[2] BGI Res, Shenzhen Key Lab Genom, Guangdong Prov Key Lab Human Dis Genom, Shenzhen 518083, Peoples R China
[3] Chinese Acad Sci, Hangzhou Inst Med HIM, HIM BGI Om Ctr, Hangzhou 310030, Peoples R China
基金
中国国家自然科学基金;
关键词
MIXED LINEAGE KINASE; FADD-DEPENDENT APOPTOSIS; DOMAIN-LIKE PROTEIN; INFLAMMATORY CASPASES; GASDERMIN D; MOLECULAR-MECHANISMS; NLRP3; INFLAMMASOME; DENDRITIC CELLS; SERUM-LEVELS; CANCER;
D O I
10.1038/s41420-025-02376-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell death is critical in tumor biology. The common cancer therapies can cause cell death and alleviate tumor, while the cancer cells can develop a resistance to cell death and survive from the therapies. Thus, not only observing the alternative mechanisms of tumor cells resistant to cell death, but also understanding the intricate dynamics of cell death processes within the tumor microenvironment (TME), are essential for tailoring effective therapeutic strategies. High-throughput sequencing technologies have revolutionized cancer research by enabling comprehensive molecular profiling. Recent advances in single cell sequencing have unraveled the heterogeneity of TME components, shedding light on their complex interactions. In this review, we explored the interplay between cell death signaling and the TME, summarised the potential drugs inducing cell death in pre-clinical stage, reviewed some studies applying next-generation sequencing technologies in cancer death research, and discussed the future utilization of updated sequencing platforms in screening novel treatment methods targeted cell death. In conclusion, leveraging multi-omics technologies to dissect cell death signaling in the context of the TME holds great promise for advancing cancer research and therapy development.
引用
收藏
页数:17
相关论文
共 213 条
[1]   Vaccination with Necroptotic Cancer Cells Induces Efficient Anti-tumor Immunity [J].
Aaes, Tania Love ;
Kaczmarek, Agnieszka ;
Delvaeye, Tinneke ;
De Craene, Bram ;
De Koker, Stefaan ;
Heyndrickx, Liesbeth ;
Delrue, Iris ;
Taminau, Joachim ;
Wiernicki, Bartosz ;
De Groote, Philippe ;
Garg, Abhishek D. ;
Leybaert, Luc ;
Grooten, Johan ;
Bertrand, Mathieu J. M. ;
Agostinis, Patrizia ;
Berx, Geert ;
Declercq, Wim ;
Vandenabeele, Peter ;
Krysko, Dmitri V. .
CELL REPORTS, 2016, 15 (02) :274-287
[2]   Inflammatory Stimuli Regulate Caspase Substrate Profiles [J].
Agard, Nicholas J. ;
Maltby, David ;
Wells, James A. .
MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (05) :880-893
[3]   Adult Glioblastoma [J].
Alexander, Brian M. ;
Cloughesy, Timothy F. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (21) :2402-+
[4]   Ferroptosis at the crossroads of cancer-acquired drug resistance and immune evasion [J].
Angeli, Jose Pedro Friedmann ;
Krysko, Dmitri, V ;
Conrad, Marcus .
NATURE REVIEWS CANCER, 2019, 19 (07) :405-414
[5]   The regulation and function of Class III PI3Ks: novel roles for Vps34 [J].
Backer, Jonathan M. .
BIOCHEMICAL JOURNAL, 2008, 410 (01) :1-17
[6]   Cytokine networks and their association with Helicobacter pylori infection in gastric carcinoma [J].
Bagheri, Vahid ;
Memar, Bahram ;
Momtazi, Amir Abbas ;
Sahebkar, Amirhossein ;
Gholamin, Mehran ;
Abbaszadegan, Mohammad Reza .
JOURNAL OF CELLULAR PHYSIOLOGY, 2018, 233 (04) :2791-2803
[7]   NLRP3 inflammasome activation downstream of cytoplasmic LPS recognition by both caspase-4 and caspase-5 [J].
Baker, Paul J. ;
Boucher, Dave ;
Bierschenk, Damien ;
Tebartz, Christina ;
Whitney, Paul G. ;
D'Silva, Damian B. ;
Tanzer, Maria C. ;
Monteleone, Mercedes ;
Robertson, Avril A. B. ;
Cooper, Matthew A. ;
Alvarez-Diaz, Silvia ;
Herold, Marco J. ;
Bedoui, Sammy ;
Schroder, Kate ;
Masters, Seth L. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2015, 45 (10) :2918-2926
[8]   Heavy and Trace Metals in Carcinoma of the Gallbladder [J].
Basu, Somprakas ;
Singh, Manish K. ;
Singh, Tej B. ;
Bhartiya, Satyanam K. ;
Singh, Sureshwar P. ;
Shukla, Vijay K. .
WORLD JOURNAL OF SURGERY, 2013, 37 (11) :2641-2646
[9]   Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm [J].
Biswas, Subhra K. ;
Mantovani, Alberto .
NATURE IMMUNOLOGY, 2010, 11 (10) :889-896
[10]   Defining the human copper proteome and analysis of its expression variation in cancers [J].
Blockhuys, S. ;
Celauro, E. ;
Hildesjo, C. ;
Feizi, A. ;
Stal, O. ;
Fierro-Gonzalez, J. C. ;
Wittung-Stafshede, P. .
METALLOMICS, 2017, 9 (02) :112-123