scholarly journals Selective Targeting of Cancer Stem Cells by 2-Aminodihydroquinoline Analogs

2017 ◽  
Vol 65 (4) ◽  
pp. 349-355
Author(s):  
Heejoo Park ◽  
Yeongji Yu ◽  
Hyejin Kim ◽  
Eun Lee ◽  
Hani Lee ◽  
...  
2017 ◽  
Vol 24 (7) ◽  
pp. 833-844.e9 ◽  
Author(s):  
Yannick D. Benoit ◽  
Ryan R. Mitchell ◽  
Ruth M. Risueño ◽  
Luca Orlando ◽  
Borko Tanasijevic ◽  
...  

Cancers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 203 ◽  
Author(s):  
Jun Ki Kim ◽  
Mi Ran Byun ◽  
Chi Hoon Maeng ◽  
Yi Rang Kim ◽  
Jin Woo Choi

Targeting cancer stem cells (CSCs) without damaging normal stem cells could contribute to the development of novel radical cancer therapies. Cells expressing leucine-rich repeat-containing G-protein coupled receptor 5 (Lgr5) constitute a cancer-causing population in the colon; therefore, targeting of Lgr5+ cells is expected to provide an opportunity to mitigate colon cancer. However, the expression of Lgr5 in normal stem cells makes it difficult to prove the efficacy of therapies targeted exclusively at Lgr5+ cancer cells. We used a modified photodynamic therapy technique involving cellular radiative transfer between green fluorescent protein (GFP)-expressing cells and a rose bengal photosensitizer. After treatment, tumors containing GFP-Lgr5+ cells were observed to be significantly suppressed or retarded with little effect on GFP-Lgr5+ stem cells at the crypt bottom. Lgr5+ CSCs were specifically eradicated in situ, when localized based on the depth from the colon lumen, revealing the potential preventive efficacy of Lgr5-targeted therapy on tumor growth. This study supports the idea that Lgr5+ cells localized near the colon luminal surface are central to colorectal cancer. With further development, the targeting of localized Lgr5+ cancer stem cells, which this study demonstrates in concept, may be feasible for prevention of colon cancer in high-risk populations.


2021 ◽  
Vol 14 (7) ◽  
pp. 676
Author(s):  
Piyush Kumar Gupta ◽  
Mrunmayee Saraff ◽  
Rekha Gahtori ◽  
Nidhi Negi ◽  
Surya Kant Tripathi ◽  
...  

The presence of small subpopulations of cells within tumor cells are known as cancer stem cells (CSCs). These cells have been the reason for metastasis, resistance with chemotherapy or radiotherapy, and tumor relapse in several types of cancers. CSCs underwent to epithelial–mesenchymal transition (EMT) and resulted in the development of aggressive tumors. CSCs have potential to modulate numerous signaling pathways including Wnt, Hh, and Notch, therefore increasing the stem-like characteristics of cancer cells. The raised expression of drug efflux pump and suppression of apoptosis has shown increased resistance with anti-cancer drugs. Among many agents which were shown to modulate these, the plant-derived bioactive agents appear to modulate these key regulators and were shown to remove CSCs. This review aims to comprehensively scrutinize the preclinical and clinical studies demonstrating the effects of phytocompounds on CSCs isolated from various tumors. Based on the available convincing literature from preclinical studies, with some clinical data, it is apparent that selective targeting of CSCs with plants, plant preparations, and plant-derived bioactive compounds, termed phytochemicals, may be a promising strategy for the treatment of relapsed cancers.


MedChemComm ◽  
2017 ◽  
Vol 8 (1) ◽  
pp. 67-72 ◽  
Author(s):  
Calabrese Gianpiero ◽  
Daou Anis ◽  
Rova Aikaterini ◽  
Tseligka Eirini ◽  
Vizirianakis S. Ioannis ◽  
...  

To limit the incidence of relapse, cancer treatments must not promote the emergence of drug resistance in tumour and cancer stem cells.


2018 ◽  
Vol 17 (7) ◽  
pp. 1475-1485 ◽  
Author(s):  
Jing Cao ◽  
Chong Li ◽  
Xiaohui Wei ◽  
Meiqing Tu ◽  
Yan Zhang ◽  
...  

BioDrugs ◽  
2007 ◽  
Vol 21 (5) ◽  
pp. 299-310 ◽  
Author(s):  
Hasan Korkaya ◽  
Max S Wicha

2019 ◽  
Author(s):  
J Gogolok ◽  
E Seidel ◽  
A Strönisch ◽  
A Reutzel-Selke ◽  
A Andreou ◽  
...  
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