Cancer Stem Cells Connecting to Immunotherapy: Key Insights, Challenges, and Potential Treatment Opportunities

被引:0
作者
Mathan, Sivapar V. [1 ]
Singh, Rana P. [1 ,2 ,3 ]
机构
[1] Jawaharlal Nehru Univ, Sch Life Sci, Canc Biol Lab, New Delhi 110067, India
[2] Gautam Buddha Univ, Dept Biotechnol, Greater Noida 201312, India
[3] Univ Colorado, Skaggs Sch Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, Anschutz Med Campus, Aurora, CO 80045 USA
关键词
cancer stem cells (CSCs); CSC niche; tumor microenvironment (TME); immunotherapy; immune evasion; TUMOR-ASSOCIATED MACROPHAGES; ACUTE MYELOID-LEUKEMIA; IL-3; RECEPTOR-ALPHA; REGULATORY T-CELLS; GROWTH-FACTOR-I; SUPPRESSOR-CELLS; INITIATING CELLS; DENDRITIC CELLS; OVARIAN-CANCER; METABOLIC CHECKPOINT;
D O I
10.3390/cancers17132100
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer continues to pose a significant challenge to global health, resulting in millions of deaths annually despite advancements in treatments like surgery, chemotherapy, and radiotherapy. A key factor complicating successful outcomes is the presence of cancer stem cells (CSCs), which possess distinctive features that facilitate tumor initiation and progression as well as resistance to therapies. These cells are adept at evading conventional treatments and can hinder the effectiveness of immunotherapy, often manipulating the tumor microenvironment to suppress immune responses. This review delves into the complex interplay between CSCs and immune cells, emphasizing their contributions to tumor heterogeneity and therapeutic resistance. By investigating the CSC niche in which these cells thrive and their complex interactions with the immune system, we aim to reveal new therapeutic avenues that could enhance patient outcomes and minimize the risk of recurrence. CSCs are characterized by remarkable self-renewal and plasticity, allowing them to transition between stem-like and differentiated states in response to various stimuli. Their existence within the CSC niche confers immune protection and maintains stem-like properties while promoting immune evasion. Activating key signaling pathways and specific surface markers is crucial in developing CSC traits, pointing to potential strategies for effective tumor eradication. Conventional therapies often fail to eliminate CSCs, which can lead to tumor recurrence. Therefore, innovative immunotherapeutic strategies such as dendritic cell vaccines (DC vaccines), chimeric antigen receptor (CAR) engineered T cells, and immune checkpoint inhibitors (ICIs) are under examination. This review sheds light on CSC's roles across different malignancies, highlighting the necessity for innovative targeted approaches in cancer treatment.
引用
收藏
页数:44
相关论文
共 359 条
[1]   Quiescent Tissue Stem Cells Evade Immune Surveillance [J].
Agudo, Judith ;
Park, Eun Sook ;
Rose, Samuel A. ;
Alibo, Eziwoma ;
Sweeney, Robert ;
Dhainaut, Maxime ;
Kobayashi, Koichi S. ;
Sachidanandam, Ravi ;
Baccarini, Alessia ;
Merad, Miriam ;
Brown, Brian D. .
IMMUNITY, 2018, 48 (02) :271-+
[2]   Research Status and Outlook of PD-1/PD-L1 Inhibitors for Cancer Therapy [J].
Ai, Leilei ;
Chen, Jian ;
Yan, Hao ;
He, Qiaojun ;
Luo, Peihua ;
Xu, Zhifei ;
Yang, Xiaochun .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2020, 14 :3625-3649
[3]   Myeloid-derived suppressor cells endow stem-like qualities to multiple myeloma cells by inducing piRNA-823 expression and DNMT3B activation [J].
Ai, Lisha ;
Mu, Shidai ;
Sun, Chunyan ;
Fan, Fengjuan ;
Yan, Han ;
Qin, You ;
Cui, Guohui ;
Wang, Yadan ;
Guo, Tao ;
Mei, Heng ;
Wang, Huafang ;
Hu, Yu .
MOLECULAR CANCER, 2019, 18 (1)
[4]   Multifunctionalized iron oxide nanoparticles for selective drug delivery to CD44-positive cancer cells [J].
Aires, Antonio ;
Ocampo, Sandra M. ;
Simoes, Bruno M. ;
Josefa Rodriguez, Maria ;
Cadenas, Jael F. ;
Couleaud, Pierre ;
Spence, Katherine ;
Latorre, Alfonso ;
Miranda, Rodolfo ;
Somoza, Alvaro ;
Clarke, Robert B. ;
Carrascosa, Jose L. ;
Cortajarena, Aitziber L. .
NANOTECHNOLOGY, 2016, 27 (06)
[5]   Aggressive serous epithelial ovarian cancer is potentially propagated by EpCAM+CD45+ phenotype [J].
Akhter, Md Zahid ;
Sharawat, Surender K. ;
Kumar, Vikash ;
Kochat, Veena ;
Equbal, Zaffar ;
Ramakrishnan, Mallika ;
Kumar, Umesh ;
Mathur, Sandeep ;
Kumar, Lalit ;
Mukhopadhyay, Asok .
ONCOGENE, 2018, 37 (16) :2089-2103
[6]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[7]   PD-L1 promotes OCT4 and Nanog expression in breast cancer stem cells by sustaining PI3K/AKT pathway activation [J].
Almozyan, Sheema ;
Colak, Dilek ;
Mansour, Fatmah ;
Alaiya, Ayodele ;
Al-Harazi, Olfat ;
Qattan, Amal ;
Al-Mohanna, Falah ;
Al-Alwan, Monther ;
Ghebeh, Hazem .
INTERNATIONAL JOURNAL OF CANCER, 2017, 141 (07) :1402-1412
[8]   NK Cells Preferentially Target Tumor Cells with a Cancer Stem Cell Phenotype [J].
Ames, Erik ;
Canter, Robert J. ;
Grossenbacher, Steven K. ;
Mac, Stephanie ;
Chen, Mingyi ;
Smith, Rachel C. ;
Hagino, Takeshi ;
Perez-Cunningham, Jessica ;
Sckisel, Gail D. ;
Urayama, Shiro ;
Monjazeb, Arta M. ;
Fragoso, Ruben C. ;
Sayers, Thomas J. ;
Murphy, William J. .
JOURNAL OF IMMUNOLOGY, 2015, 195 (08) :4010-4019
[9]   Tumor morphology and phenotypic evolution driven by selective pressure from the microenvironment [J].
Anderson, Alexander R. A. ;
Weaver, Alissa M. ;
Cummings, Peter T. ;
Quaranta, Vito .
CELL, 2006, 127 (05) :905-915
[10]   Intraperitoneal immunotherapy with T cells stably and transiently expressing anti-EpCAM CAR in xenograft models of peritoneal carcinomatosis [J].
Ang, Wei Xia ;
Li, Zhendong ;
Chi, Zhixia ;
Du, Shou-Hui ;
Chen, Can ;
Tay, Johan C. K. ;
Toh, Han Chong ;
Connolly, John E. ;
Xu, Xue Hu ;
Wang, Shu .
ONCOTARGET, 2017, 8 (08) :13545-13559