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Review
. 1994 Oct 25;91(22):10251-4.
doi: 10.1073/pnas.91.22.10251.

Inducing differentiation of transformed cells with hybrid polar compounds: a cell cycle-dependent process

Affiliations
Review

Inducing differentiation of transformed cells with hybrid polar compounds: a cell cycle-dependent process

P A Marks et al. Proc Natl Acad Sci U S A. .

Abstract

Transformed cells do not necessarily lose their capacity to differentiate. Various agents can induce many types of neoplastic cells to terminal differentiation. Among such inducers, a particularly potent group consists of hybrid polar compounds; hexamethylene bisacetamide (HMBA) is the prototype of this group. With virus-transformed murine erythroleukemia cells as a model, HMBA was shown to cause these cells to arrest in G1 phase and express globin genes. This review focuses on HMBA-induced modulation of factors regulating G1-to-S phase progression, including a decrease in the G1 cyclin-dependent kinase cdk4, associated with inhibition of phosphorylation of the retinoblastoma protein pRB and possibly other related proteins that, in turn, sequester factors required for initiation of DNA synthesis; this provides a possible mechanism for HMBA-induced terminal cell division. Evidence that hybrid polar compounds have therapeutic potential for cancer treatment will also be reviewed.

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References

    1. Nature. 1988 Jul 14;334(6178):124-9 - PubMed
    1. Proc Natl Acad Sci U S A. 1987 Aug;84(15):5282-6 - PubMed
    1. Cancer Res. 1988 Dec 15;48(24 Pt 1):7304-9 - PubMed
    1. Science. 1989 Feb 17;243(4893):934-7 - PubMed
    1. Proc Natl Acad Sci U S A. 1989 Aug;86(16):6358-62 - PubMed

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