Therapeutic Targeting of Cancer Stem Cells in Lung, Head and Neck, and Bladder Cancers

Resistance to cancer therapy remains a significant obstacle in treating patients with various solid malignancies. Exposure to current chemotherapeutics and targeted agents invariably leads to therapy resistance, heralding the need for novel agents. Cancer stem cells (CSCs)-a subpopulation of tumor c...

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Bibliographic Details
Main Authors: Mudra, Sarah E. (Author), Sadhukhan, Pritam (Author), Ugurlu, M. Talha (Author), Alam, Shorna (Author), Hoque, Mohammad O. (Author)
Format: Article
Language:English
Published: Multidisciplinary Digital Publishing Institute, 2022-01-21T16:41:17Z.
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Online Access:Get fulltext
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100 1 0 |a Mudra, Sarah E.  |e author 
700 1 0 |a Sadhukhan, Pritam  |e author 
700 1 0 |a Ugurlu, M. Talha  |e author 
700 1 0 |a Alam, Shorna  |e author 
700 1 0 |a Hoque, Mohammad O.  |e author 
245 0 0 |a Therapeutic Targeting of Cancer Stem Cells in Lung, Head and Neck, and Bladder Cancers 
260 |b Multidisciplinary Digital Publishing Institute,   |c 2022-01-21T16:41:17Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/133177.2 
520 |a Resistance to cancer therapy remains a significant obstacle in treating patients with various solid malignancies. Exposure to current chemotherapeutics and targeted agents invariably leads to therapy resistance, heralding the need for novel agents. Cancer stem cells (CSCs)-a subpopulation of tumor cells with capacities for self-renewal and multi-lineage differentiation-represent a pool of therapeutically resistant cells. CSCs often share physical and molecular characteristics with the stem cell population of the human body. It remains challenging to selectively target CSCs in therapeutically resistant tumors. The generation of CSCs and induction of therapeutic resistance can be attributed to several deregulated critical growth regulatory signaling pathways such as WNT/β-catenin, Notch, Hippo, and Hedgehog. Beyond growth regulatory pathways, CSCs also change the tumor microenvironment and resist endogenous immune attack. Thus, CSCs can interfere with each stage of carcinogenesis from malignant transformation to the onset of metastasis to tumor recurrence. A thorough review of novel targeted agents to act against CSCs is fundamental for advancing cancer treatment in the setting of both intrinsic and acquired resistance. 
655 7 |a Article 
773 |t Cancers