Literature DB >> 6683114

Unbalanced cell growth and increased protein synthesis induced by chemotherapeutic agents.

D W Ross.   

Abstract

Unbalanced cell growth as manifested by an increase in cellular volume and in cellular dry mass following exposure to a variety of chemotherapeutic agents has been shown for neoplastic cells in vitro and human leukemic cells in vivo. The purpose of the present investigation was to test the hypothesis that unbalanced cell growth results from a disassociation of cell growth and cell division due to the blocking effect of chemotherapeutic agents. Monolayer cultures of CHO fibroblasts were studied in terms of their response to two chemotherapeutic agents that differ significantly in their mode of action, adriamycin and chlorambucil. Following exposure to these drugs, cell volume increased at a rate of from 1% to 4% per h; the total cell protein increased at a rate of from 4% to 7% per h. These changes were observed in both log and stationary phase cultures. Thus exposure to adriamycin and chlorambucil was followed by a more rapid rate of protein synthesis relative to the rate of degradation, resulting in larger cells with more protein whether or not the cells were actively in the division cycle. This is inconsistent with the hypothesis that unbalanced growth results simply from a disassociation of the cell division cycle from cell growth. These observations suggest that a final common pathway in the mode of action of chemotherapeutic agents may be the induction of unscheduled protein synthesis resulting in unbalanced cell growth.

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Year:  1983        PMID: 6683114

Source DB:  PubMed          Journal:  Blood Cells        ISSN: 0340-4684


  6 in total

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2.  Cell death induced in L-cells by treatment with thymidine: staging of the process and relationship to apoptosis.

Authors:  J S Amenta; M J Sargus; F M Baccino; C Sacchi; G Bonelli
Journal:  In Vitro Cell Dev Biol Anim       Date:  1993-11       Impact factor: 2.416

3.  An efficient multiple-exposure analysis of the toxicity of crisnatol, a DNA intercalator in phase II clinical trials.

Authors:  R M Zucker; D J Adams; K W Bair; K H Elstein
Journal:  Invest New Drugs       Date:  1992-04       Impact factor: 3.850

4.  Single cell monitoring of growth arrest and morphological changes induced by transfer of wild-type p53 alleles to glioblastoma cells.

Authors:  E G Van Meir; K Roemer; A C Diserens; T Kikuchi; S A Rempel; M Haas; H J Huang; T Friedmann; N de Tribolet; W K Cavenee
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-14       Impact factor: 11.205

5.  Restriction of protein synthesis abolishes senescence features at cellular and organismal levels.

Authors:  Yuki Takauji; Takumi Wada; Asuka Takeda; Ikuru Kudo; Kensuke Miki; Michihiko Fujii; Dai Ayusawa
Journal:  Sci Rep       Date:  2016-01-05       Impact factor: 4.379

6.  Lamin B receptor plays a key role in cellular senescence induced by inhibition of the proteasome.

Authors:  Atsuki En; Yuki Takauji; Kensuke Miki; Dai Ayusawa; Michihiko Fujii
Journal:  FEBS Open Bio       Date:  2020-01-06       Impact factor: 2.792

  6 in total

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