Vitamin D and differentiation in cancer

This paper reviews the current understanding of the vitamin D-induced differentiation of neoplastic cells, which results in the generation of cells that acquire near-normal, mature phenotype. Examples of the criteria by which differentiation is recognized in each cell type are provided, and only tho...

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Published in:Critical reviews in clinical laboratory sciences Vol. 46; no. 4; pp. 190 - 209
Main Authors: Gocek, Elzbieta, Studzinski, George P.
Format: Journal Article
Language:English
Published: England Informa UK Ltd 01-01-2009
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Abstract This paper reviews the current understanding of the vitamin D-induced differentiation of neoplastic cells, which results in the generation of cells that acquire near-normal, mature phenotype. Examples of the criteria by which differentiation is recognized in each cell type are provided, and only those effects of 1α,25-dihydroxyvitamin D3 (1,25D) on cell proliferation and survival that are associated with the differentiation process are emphasized. The existing knowledge, often fragmentary, of the signaling pathways that lead to vitamin D-induced differentiation of colon, breast, prostate, squamous cell carcinoma, osteosarcoma, and myeloid leukemia cancer cells is outlined. The important distinctions between the different mechanisms of 1,25D-induced differentiation that are cell-type and cell-context specific are pointed out where known. There is a considerable body of evidence that the principal human cancer cells can be suitable candidates for chemoprevention or differentiation therapy with vitamin D. However, further studies are needed to fully understand the underlying mechanisms in order to improve the therapeutic approaches.
AbstractList This paper reviews the current understanding of the vitamin D-induced differentiation of neoplastic cells, which results in the generation of cells that acquire near-normal, mature phenotype. Examples of the criteria by which differentiation is recognized in each cell type are provided, and only those effects of 1α,25-dihydroxyvitamin D 3 (1,25D) on cell proliferation and survival that are associated with the differentiation process are emphasized. The existing knowledge, often fragmentary, of the signaling pathways that lead to vitamin D-induced differentiation of colon, breast, prostate, squamous cell carcinoma, osteosarcoma, and myeloid leukemia cancer cells is outlined. The important distinctions between the different mechanisms of 1,25D-induced differentiation that are cell-type and cell-context specific are pointed out where known. There is a considerable body of evidence that the principal human cancer cells can be suitable candidates for chemoprevention or differentiation therapy with vitamin D. However, further studies are needed to fully understand the underlying mechanisms in order to improve the therapeutic approaches.
This paper reviews the current understanding of the vitamin D-induced differentiation of neoplastic cells, which results in the generation of cells that acquire near-normal, mature phenotype. Examples of the criteria by which differentiation is recognized in each cell type are provided, and only those effects of 1α,25-dihydroxyvitamin D3 (1,25D) on cell proliferation and survival that are associated with the differentiation process are emphasized. The existing knowledge, often fragmentary, of the signaling pathways that lead to vitamin D-induced differentiation of colon, breast, prostate, squamous cell carcinoma, osteosarcoma, and myeloid leukemia cancer cells is outlined. The important distinctions between the different mechanisms of 1,25D-induced differentiation that are cell-type and cell-context specific are pointed out where known. There is a considerable body of evidence that the principal human cancer cells can be suitable candidates for chemoprevention or differentiation therapy with vitamin D. However, further studies are needed to fully understand the underlying mechanisms in order to improve the therapeutic approaches. [PUBLICATION ABSTRACT]
This paper reviews the current understanding of the vitamin D-induced differentiation of neoplastic cells, which results in the generation of cells that acquire near-normal, mature phenotype. Examples of the criteria by which differentiation is recognized in each cell type are provided, and only those effects of 1α,25-dihydroxyvitamin D3 (1,25D) on cell proliferation and survival that are associated with the differentiation process are emphasized. The existing knowledge, often fragmentary, of the signaling pathways that lead to vitamin D-induced differentiation of colon, breast, prostate, squamous cell carcinoma, osteosarcoma, and myeloid leukemia cancer cells is outlined. The important distinctions between the different mechanisms of 1,25D-induced differentiation that are cell-type and cell-context specific are pointed out where known. There is a considerable body of evidence that the principal human cancer cells can be suitable candidates for chemoprevention or differentiation therapy with vitamin D. However, further studies are needed to fully understand the underlying mechanisms in order to improve the therapeutic approaches.
This paper reviews the current understanding of the vitamin D-induced differentiation of neoplastic cells, which results in the generation of cells that acquire near-normal, mature phenotype. Examples of the criteria by which differentiation is recognized in each cell type are provided, and only those effects of 1alpha,25-dihydroxyvitamin D(3) (1,25D) on cell proliferation and survival that are associated with the differentiation process are emphasized. The existing knowledge, often fragmentary, of the signaling pathways that lead to vitamin D-induced differentiation of colon, breast, prostate, squamous cell carcinoma, osteosarcoma, and myeloid leukemia cancer cells is outlined. The important distinctions between the different mechanisms of 1,25D-induced differentiation that are cell-type and cell-context specific are pointed out where known. There is a considerable body of evidence that the principal human cancer cells can be suitable candidates for chemoprevention or differentiation therapy with vitamin D. However, further studies are needed to fully understand the underlying mechanisms in order to improve the therapeutic approaches.
Author Studzinski, George P.
Gocek, Elzbieta
AuthorAffiliation 1 Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland
2 Department of Pathology and Laboratory Medicine, UMDNJ-New Jersey Medical School, Newark, NJ, USA
AuthorAffiliation_xml – name: 2 Department of Pathology and Laboratory Medicine, UMDNJ-New Jersey Medical School, Newark, NJ, USA
– name: 1 Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland
Author_xml – sequence: 1
  givenname: Elzbieta
  surname: Gocek
  fullname: Gocek, Elzbieta
  email: studzins@umdnj.edu
  organization: 1Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland
– sequence: 2
  givenname: George P.
  surname: Studzinski
  fullname: Studzinski, George P.
  email: studzins@umdnj.edu
  organization: 1Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland
BackLink https://www.ncbi.nlm.nih.gov/pubmed/19650715$$D View this record in MEDLINE/PubMed
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content type line 23
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Referee Dr David M. Goldberg, Department of Pathobiology and Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada
OpenAccessLink https://europepmc.org/articles/pmc2820234?pdf=render
PMID 19650715
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PublicationCentury 2000
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PublicationTitle Critical reviews in clinical laboratory sciences
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Snippet This paper reviews the current understanding of the vitamin D-induced differentiation of neoplastic cells, which results in the generation of cells that...
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SubjectTerms Animals
Calcitriol - pharmacology
Cancer
Cell Differentiation - drug effects
Cells
Chemotherapy
Differentiation
Genotype & phenotype
Humans
myeloid leukemia
Neoplasms - drug therapy
Neoplasms - pathology
Signal transduction
signaling pathways
solid tumors
Vitamin D
Title Vitamin D and differentiation in cancer
URI https://www.tandfonline.com/doi/abs/10.1080/10408360902982128
https://www.ncbi.nlm.nih.gov/pubmed/19650715
https://www.proquest.com/docview/204164883
https://search.proquest.com/docview/67550522
https://pubmed.ncbi.nlm.nih.gov/PMC2820234
Volume 46
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