scholarly journals The Role of the Hedgehog Pathway in Chemoresistance of Gastrointestinal Cancers

Cells ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 2030
Author(s):  
Yabing Liang ◽  
Ling Yang ◽  
Jingwu Xie

The hedgehog pathway, which plays a significant role in embryonic development and stem cell regulation, is activated in gastrointestinal cancers. Chemotherapy is widely used in cancer treatment. However, chemoresistance becomes a substantial obstacle in cancer therapy. This review focuses on the recent advances in the hedgehog pathway’s roles in drug resistance of gastrointestinal cancers and the novel drugs and strategies targeting hedgehog signaling.

Blood ◽  
2014 ◽  
Vol 124 (13) ◽  
pp. 2061-2071 ◽  
Author(s):  
Zhiqiang Liu ◽  
Jingda Xu ◽  
Jin He ◽  
Yuhuan Zheng ◽  
Haiyan Li ◽  
...  

Key Points CD138+ MM cells are a major source of SHH. Autocrine SHH enhances MM drug resistance.


Oncogenesis ◽  
2017 ◽  
Vol 6 (1) ◽  
pp. e291-e291 ◽  
Author(s):  
T Redmer ◽  
I Walz ◽  
B Klinger ◽  
S Khouja ◽  
Y Welte ◽  
...  

Nutrients ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1798 ◽  
Author(s):  
Mariarosaria Negri ◽  
Annalisa Gentile ◽  
Cristina de Angelis ◽  
Tatiana Montò ◽  
Roberta Patalano ◽  
...  

Increasing interest in studying the role of vitamin D in cancer has been provided by the scientific literature during the last years, although mixed results have been reported. Vitamin D deficiency has been largely associated with various types of solid and non-solid human cancers, and the almost ubiquitous expression of vitamin D receptor (VDR) has always led to suppose a crucial role of vitamin D in cancer. However, the association between vitamin D levels and the risk of solid cancers, such as colorectal, prostate and breast cancer, shows several conflicting results that raise questions about the use of vitamin D supplements in cancer patients. Moreover, studies on vitamin D supplementation do not always show improvements in tumor progression and mortality risk, particularly for prostate and breast cancer. Conversely, several molecular studies are in agreement about the role of vitamin D in inhibiting tumor cell proliferation, growth and invasiveness, cell cycle arrest and inflammatory signaling, through which vitamin D may also regulate cancer microenvironment through the activation of different molecular pathways. More recently, a role in the regulation of cancer stem cells proliferation and short non-coding microRNA (miRNAs) expression has emerged, conferring to vitamin D a more crucial role in cancer development and progression. Interestingly, it has been shown that vitamin D is able not only to potentiate the effects of traditional cancer therapy but can even contribute to overcome the molecular mechanisms of drug resistance—often triggering tumor-spreading. At this regard, vitamin D can act at various levels through the regulation of growth of cancer stem cells and the epithelial–mesenchymal transition (EMT), as well as through the modulation of miRNA gene expression. The current review reconsiders epidemiological and molecular literature concerning the role of vitamin D in cancer risk and tumor development and progression, as well as the action of vitamin D supplementation in potentiating the effects of drug therapy and overcoming the mechanisms of resistance often triggered during cancer therapies, by critically addressing strengths and weaknesses of available data from 2010 to 2020.


Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4764
Author(s):  
Umbreen Hafeez ◽  
Sagun Parakh ◽  
Hui K. Gan ◽  
Andrew M. Scott

Antibody–drug conjugates (ADCs) are novel drugs that exploit the specificity of a monoclonal antibody (mAb) to reach target antigens expressed on cancer cells for the delivery of a potent cytotoxic payload. ADCs provide a unique opportunity to deliver drugs to tumor cells while minimizing toxicity to normal tissue, achieving wider therapeutic windows and enhanced pharmacokinetic/pharmacodynamic properties. To date, nine ADCs have been approved by the FDA and more than 80 ADCs are under clinical development worldwide. In this paper, we provide an overview of the biology and chemistry of each component of ADC design. We briefly discuss the clinical experience with approved ADCs and the various pathways involved in ADC resistance. We conclude with perspectives about the future development of the next generations of ADCs, including the role of molecular imaging in drug development.


2017 ◽  
Vol 233 (4) ◽  
pp. 2871-2881 ◽  
Author(s):  
Amir A. Momtazi-borojeni ◽  
Elham Abdollahi ◽  
Faezeh Ghasemi ◽  
Michele Caraglia ◽  
Amirhossein Sahebkar
Keyword(s):  

2019 ◽  
Vol 21 (Supplement_6) ◽  
pp. vi195-vi195
Author(s):  
Arabinda Das ◽  
Ramin Eskandari ◽  
Mohammed Alshareef ◽  
Libby Kosnik Infinger ◽  
Sunil Patel ◽  
...  

Abstract Brain tumors are the leading cause of childhood cancer mortality, with medulloblastoma (MB) representing the most frequent malignant tumor. The identification of cancer stem cell (CSC) populations in MB has play a vital role in drug resistance, and cancer relapse. Galectin-3 (Gal-3) a multifunctional β-galactoside-binding protein is known to participate in tumor progression and drug resistance. However, the exact role of Gal-3 in medulloblastoma tumor pathophysiology is yet unknown. In this study, we observed higher levels of stem/progenitor cell markers, such as Oct4, Sox2, CD133 and Nanog in MB slices. Among the Gal family, Gal-3 in particular was highly expressed in MB tumor slices. To further investigate Gal-3’s role in the pathophysiology of MB, we used either small interfering RNA (siRNA) to knock down Gal-3 expression or Gal-3 inhibitor, TD139 to suppress Gal-3 expression in ex vivo slice culture model. Upon suppressing Gal-3 in parental MB slices, drug resistance (MDR1and MPR1) and stem cell related gene expression were all significantly decreased. Furthermore, CXCL6, CXCL7 and CXCR2 were down-regulated in Gal-3-knockdown or Gal-3 inhibitor treated MB tumor slices, while CXCR2 overexpression in Gal-3-knockdown or Gal-3 inhibitor treated MB slices restored their viability. These results indicate that highly expressed Gal-3 may up-regulate CXCR2 to augment MB invasiveness and progression. Gal-3 may be a prognostic and innovative target for the treatment of MB.


2017 ◽  
Vol 2017 ◽  
pp. 1-14 ◽  
Author(s):  
Ana Almazán-Moga ◽  
Patricia Zarzosa ◽  
Isaac Vidal ◽  
Carla Molist ◽  
Irina Giralt ◽  
...  

Rhabdomyosarcoma (RMS) is the most common type of soft tissue sarcoma in children and can be divided into two main subtypes: embryonal (eRMS) and alveolar (aRMS). Among the cellular heterogeneity of tumors, the existence of a small fraction of cells called cancer stem cells (CSC), thought to be responsible for the onset and propagation of cancer, has been demonstrated in some neoplasia. Although the existence of CSC has been reported for eRMS, their existence in aRMS, the most malignant subtype, has not been demonstrated to date. Given the lack of suitable markers to identify this subpopulation in aRMS, we used cancer stem cell-enriched supracellular structures (spheres and holoclones) to study this subpopulation. This strategy allowed us to demonstrate the capacity of both aRMS and eRMS cells to form these structures and retain self-renewal capacity. Furthermore, cells contained in spheres and holoclones showed significant Hedgehog pathway induction, the inhibition of which (pharmacologic or genetic) impairs the formation of both holoclones and spheres. Our findings point to a crucial role of this pathway in the maintenance of these structures and suggest that Hedgehog pathway targeting in CSC may have great potential in preventing local relapses and metastases.


2021 ◽  
Vol 118 (16) ◽  
pp. e2021251118
Author(s):  
Andy Chan ◽  
Sophia Ma ◽  
Bret J. Pearson ◽  
Danny Chan

The extracellular matrix (ECM) provides a precise physical and molecular environment for cell maintenance, self-renewal, and differentiation in the stem cell niche. However, the nature and organization of the ECM niche is not well understood. The adult freshwater planarian Schmidtea mediterranea maintains a large population of multipotent stem cells (neoblasts), presenting an ideal model to study the role of the ECM niche in stem cell regulation. Here we tested the function of 165 planarian homologs of ECM and ECM-related genes in neoblast regulation. We identified the collagen gene family as one with differential effects in promoting or suppressing proliferation of neoblasts. col4-1, encoding a type IV collagen α-chain, had the strongest effect. RNA interference (RNAi) of col4-1 impaired tissue maintenance and regeneration, causing tissue regression. Finally, we provide evidence for an interaction between type IV collagen, the discoidin domain receptor, and neuregulin-7 (NRG-7), which constitutes a mechanism to regulate the balance of symmetric and asymmetric division of neoblasts via the NRG-7/EGFR pathway.


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