Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1980;51(2):107-11.
doi: 10.1007/BF00690451.

Characterization of cell cycle and biological parameters of transplantable glioma cell lines and clones

Characterization of cell cycle and biological parameters of transplantable glioma cell lines and clones

L Ko et al. Acta Neuropathol. 1980.

Abstract

Aberrant biological characteristics of established cell lines and clones, derived from nitrosourea-induced gliomas in CDF rats were compared with normal rat glial cells. Despite their tumorigenicity and unrestrained proliferation due to inherent cytogenetic anomalies, these neoplastic cells retained certain normal glial attributes to a variable degree. Differentiated glioma cells resembled normal glial cells to a greater extent than they resembled anaplastic glioma cells. They were also less malignant upon implantation. Cell cycle analyses revealed that considerable variations not only for the G1 phase but also for the S period were demonstrated among different tumor cell types. Shortening of the G1 phase may dictate a shorter generation time (shorter doubling time) since a larger potential proliferative pool may overcome the effect of a prolonged generation period may constitute a faster proliferation rate. Although the cell generation period of neoplastic cells is not necessarily shorter than that of normal glial cells, the lower proportion of nonproliferative cells results in a much faster growth rate when compared wo non-neoplastic glial cells in culture.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Cell Biol. 1967 Sep;34(3):915-6 - PubMed
    1. Exp Cell Res. 1977 Feb;104(2):255-62 - PubMed
    1. Lab Invest. 1972 Jan;26(1):74-85 - PubMed
    1. Med Biol. 1978 Aug;56(4):184-93 - PubMed
    1. Am J Pathol. 1971 Apr;63(1):37-56 - PubMed

Publication types

Substances

LinkOut - more resources