Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Therapeutic Targeting of Cancer Stem Cells in Lung, Head and Neck, and Bladder Cancers
This is not the latest version of this item. The latest version can be found here.

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

Thumbnail Image
Download
Name

cancers-13-05098.pdf

Size

14.92 MB

Format

Adobe PDF

Checksum (MD5)

77f28bc102b2ff7551a213e45b3c6adc

Download all files submitted through automated deposit
packager-61659928.zip (14.47 MB)
Author(s)
Mudra, Sarah E.
•
Sadhukhan, Pritam
•
Ugurlu, M. Talha
•
Alam, Shorna
•
Hoque, Mohammad O.
Date Issued
October 12, 2021
Publisher
Multidisciplinary Digital Publishing Institute
Citation
Cancers 13 (20): 5098 (2021)
Version
Final published version
Abstract
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.
Terms of Use
Creative Commons Attribution
https://creativecommons.org/licenses/by/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/133177
DOI of Published Version
http://dx.doi.org/10.3390/cancers13205098
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.