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血卟啉衍生物光动力疗法对结肠癌细胞黏附性的调节作用

Modulation of colonic cancer cell adhesiveness by haematoporphyrin derivative photodynamic therapy.

作者信息

Foultier M T, Vonarx-Coinsmann V, Cordel S, Combre A, Patrice T

机构信息

Physiologie, Photobiologie des Cancers, Sixième Etage, Faculté de Pharmacie, Nantes, France.

出版信息

J Photochem Photobiol B. 1994 Apr;23(1):9-17. doi: 10.1016/1011-1344(93)06975-9.

Abstract

Haematoporphyrin derivative photodynamic therapy (HPD-PDT) induces damage of plasma membranes and other cellular targets. This damage could modify the adhesiveness of cancer cells, which is an important parameter in cancer metastasis. We studied the effect of HPD alone and HPD incubation followed by argon laser light on the adhesiveness of progressive (PROb) or regressive (REGb) cancer cells of the same colonic origin. Adhesiveness was studied on plastic or endothelial cell monolayers (ECMs). In the absence of treatment, both PROb and REGb cells adhered better on plastic than on ECs. HPD alone and HPD-PDT induced toxicity proportional to the HPD dose. HPD-PDT increased the adhesiveness rate of both cell lines on plastic and decreased adhesiveness to ECs. HPD-PDT of ECMs increased adhesiveness but only for HPD doses giving at least 50% cell death. HPD alone and HPD-PDT of culture media led to an insignificant decrease in the cell adhesiveness to ECMs. As cells which are more metastatic are also more adherent, a decreased adhesiveness to ECMs after HPD-PDT suggests that PDT is a safe treatment considering metastasis.

摘要

血卟啉衍生物光动力疗法(HPD-PDT)会导致质膜及其他细胞靶点受损。这种损伤可能会改变癌细胞的黏附性,而黏附性是癌症转移中的一个重要参数。我们研究了单独使用HPD以及HPD孵育后再用氩激光照射对源自同一结肠的进展期(PROb)或消退期(REGb)癌细胞黏附性的影响。在塑料或内皮细胞单层(ECM)上研究了黏附性。在未进行处理的情况下,PROb和REGb细胞在塑料上的黏附性均优于在EC上的黏附性。单独使用HPD以及HPD-PDT所诱导的毒性与HPD剂量成正比。HPD-PDT提高了两种细胞系在塑料上的黏附率,并降低了对EC的黏附性。对ECM进行HPD-PDT可提高黏附性,但仅针对能导致至少50%细胞死亡的HPD剂量。单独使用HPD以及对培养基进行HPD-PDT导致细胞对ECM的黏附性出现不显著的降低。由于转移性更强的细胞黏附性也更强,HPD-PDT后对ECM的黏附性降低表明,考虑到转移情况,光动力疗法是一种安全的治疗方法。

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