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. Author manuscript; available in PMC: 2007 Mar 26.
Published in final edited form as: Biochim Biophys Acta. 2004 Oct 22;1711(2):208–214. doi: 10.1016/j.bbamem.2004.10.001

Table 1.

Summary of the published studies of gap junction-independent functions of connexins in cell growth and tumorigenicity

References Cell Systems Connexin types GJIC-independent functions in cell/tumor growth GJIC Connexin localization
Mesnil et al. [6] HeLa cells Cx26, Cx40, Cx43 (transfected) Cx26—cell growth inhibition; Cx 40 and Cx43—no effect GJIC for all three connexins Cx40, Cx43—cell–cell contact; Cx26—cytosol
Huang et al. [12] Human glioblastoma cells Cx43 (transfected) Inhibition on cell and tumor growth No GJIC Mainly in the nucleus and cytoplasm
Duflot-Dancer et al. [14] HeLa cells expressing Cx26 Cx26 mutants: C60F, R87L, R143W (transfected) P87L and R143W—increased tumorigenicity; C60F—no change R87L and R143W—no change; C60F—reduced Cell–cell contact area
Omori and Yamsaki [15] C6 glioma cells expressing Cx43 Dominant negative Cx43 mutants: L160M and A253V Both mutants inhibit the effect of wt Cx43 on suppression of tumor growth A253V—no inhibition on GJIC; L160M—inhibition No changes of distribution pattern
Krutovskikh et al. [16] Rat bladder carcinoma BC31 cell Dominant negative Cx43 mutants: K162A, E166G and T154Y None of the mutants had effects on cell growth; T154Y accelerated tumor growth. All three mutants blocked GJIC; T154Y—only transfer of neurobiotin Wt and T154Y in the lateral membrane; K162A and E166G in the cytoplasm.
Moorby and Patel [17] 3T3 A31 fibroblasts expressing endogenous Cx43 and Neuro2a cells with no endogenous connexins Cx43 mutants: S255A, S279A, S282A, C-terminal truncated (1–256) and C-terminal domain In 3T3 cells, S279A and S282A grew slowly; S255A faster than control; mutants affected cell growth without cell contact and GJ; In Neuro2a cells, wt Cx43 and Cx43 C-terminus, but not Cx43(1–256), suppressed cell growth without GJ. Cells expressing S255A, S279A, and S282A mutants were coupled similarly and prevent PDGF-induced loss of cell coupling in 3T3 cells. N/A
Olbina and Eckhart [18] HeLa and C6 glioma cells Second extracellular mutants of Cx43: F199L, R202E, and E205R Mutants had similar inhibition of cell growth as wt Cx43 Loss of GJIC by mutants Wt—plasma membrane; Mutants—membrane and cytoplasm
Dang et al. [19] Cardiomyocytes and HeLa cells C-terminal domain of Cx43 Inhibition of cell growth N/A Cytoplasm and nucleus
Bond et al. [13] C6 glioma cells Cx32 (transfected) Cell growth in vitro—no change; tumor growth—retarded No correlation of the function with GJIC N/A
Qin et al. [20] MDA-MB-231 Cx43 and Cx26 (retroviral delivery) Dramatic suppression of tumor growth No substantial rescue of GJIC Cytoplasm of cells and xenoplants