The effect of the PQ1 anti-breast cancer agent on normal tissues.

Anti-cancer Drugs
Ying DingThu A Nguyen

Abstract

Gap junctions are intercellular channels connecting adjacent cells, allowing cells to transport small molecules. The loss of gap junctional intercellular communication (GJIC) is one of the important hallmarks of cancer. Restoration of GJIC is related to the reduction of tumorigenesis and increase in drug sensitivity. Previous reports have shown that PQ1, a quinoline derivative, increases GJIC in T47D breast cancer cells, and subsequently attenuates xenograft breast tumor growth. Combinational treatment of PQ1 and tamoxifen can lower the effective dose of tamoxifen in cancer cells. In this study, the effects of PQ1 were examined in normal C57BL/6J mice, evaluating the distribution, toxicity, and adverse effects. The distribution of PQ1 was quantified by high-performance liquid chromatography and mass spectrometry. The expressions of survivin, caspase-8, cleaved caspase-3, aryl hydrocarbon receptor (AhR), and gap junction protein, connexin 43 (Cx43), were assessed using western blot analysis. Our results showed that PQ1 was absorbed and distributed to vital organs within 1 h and the level of PQ1 decreased after 24 h. Furthermore, PQ1 increased the expression of survivin, but decreased the expression of caspase-8 and caspase-3 act...Continue Reading

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Citations

Jun 19, 2013·PloS One·Stephanie N ShishidoThu Annelise Nguyen
Feb 18, 2016·Cancer Letters·Christina L GrekElizabeth S Yeh
Sep 17, 2013·International Journal of Cancer. Journal International Du Cancer·Stephanie N ShishidoThu Annelise Nguyen
Sep 18, 2014·The Journal of Organic Chemistry·Courtney E Meyet, Catharine H Larsen

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