Literature DB >> 7960245

Differential effects of protein kinase A sub-units on Chinese-hamster-ovary cell cycle and proliferation.

G Tortora1, S Pepe, C Bianco, V Damiano, A Ruggiero, G Baldassarre, C Corbo, Y S Cho-Chung, A R Bianco, F Ciardiello.   

Abstract

It has been shown that a marked increase in the levels of RI alpha sub-units and a decrease in RII beta sub-unit levels correlate with neoplastic transformation or with the mitogenic response of normal cells to hormones and growth factors. The selective down-regulation of RI alpha and the following induction of RII beta determine cell-growth arrest and differentiation of several cancer cells. To directly address the question whether the 2 protein-kinase-A(PKA) isoforms play different roles in the control of proliferation and cell-cycle distribution, we introduced and over-expressed the different PKA sub-units in Chinese-hamster-ovary (CHO) cells via retroviral-vector-mediated gene transfer. Whereas CHO cells treated with RI alpha anti-sense oligodeoxynucleotides were growth arrested and accumulated in the G0/G1 phases of the cell cycle, infection of CHO cells with a retroviral vector in order to over-express RI alpha determined growth advantages in monolayer conditions and substantially increased their cloning efficiency in soft agar. These events correlated with a sustained percentage of cells in S phase induced by RI alpha over-expression in the infected cells. In contrast, CHO cells infected with retroviral vectors over-expressing either a RII beta sub-unit or a C alpha catalytic sub-unit of PKA exhibited growth arrest within a few days of culture and accumulated in the G2-M phase of the cell cycle. The results of our study demonstrate that the different PKA sub-units play different and specific roles in the control of cell growth and cell-cycle distribution.

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Year:  1994        PMID: 7960245     DOI: 10.1002/ijc.2910590521

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  5 in total

1.  Over-expressed human TREK-1 inhibits CHO cell proliferation via inhibiting PKA and p38 MAPK pathways and subsequently inducing G1 arrest.

Authors:  Man Zhang; Hua-Jing Yin; Wei-Ping Wang; Jiang Li; Xiao-Liang Wang
Journal:  Acta Pharmacol Sin       Date:  2016-07-11       Impact factor: 6.150

2.  Interaction of the regulatory subunit of the cAMP-dependent protein kinase with PATZ1 (ZNF278).

Authors:  Weng-Lang Yang; Roald Ravatn; Kazuya Kudoh; Leah Alabanza; Khew-Voon Chin
Journal:  Biochem Biophys Res Commun       Date:  2009-12-22       Impact factor: 3.575

3.  Regulation of neuroblast mitosis is determined by PACAP receptor isoform expression.

Authors:  A Nicot; E DiCicco-Bloom
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-10       Impact factor: 11.205

4.  8-Cl-cAMP and PKA I-selective cAMP analogs effectively inhibit undifferentiated thyroid cancer cell growth.

Authors:  Elisa Stellaria Grassi; Alessandra Dicitore; Irene Negri; Maria Orietta Borghi; Giovanni Vitale; Luca Persani
Journal:  Endocrine       Date:  2016-07-27       Impact factor: 3.633

5.  Isoform-specific targeting of PKA to multivesicular bodies.

Authors:  Michele E Day; Guido M Gaietta; Mira Sastri; Antonius Koller; Mason R Mackey; John D Scott; Guy A Perkins; Mark H Ellisman; Susan S Taylor
Journal:  J Cell Biol       Date:  2011-04-18       Impact factor: 10.539

  5 in total

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