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雌性比目鱼(欧洲比目鱼,Platichthys flesus (L.))肝脏在污染诱导的毒性损伤和肝细胞癌发生过程中的克隆性外源性物质抗性

Clonal xenobiotic resistance during pollution-induced toxic injury and hepatocellular carcinogenesis in liver of female flounder (Platichthys flesus (L.)).

作者信息

Koehler Angela, Alpermann Tilmann, Lauritzen Bjarne, Van Noorden Cornelis J F

机构信息

Department of Ecotoxicology, Alfred Wegener Institute for Marine and Polar Research, Am Handelshafen 12, Haus C, Bremerhaven 27570, Germany.

出版信息

Acta Histochem. 2004;106(2):155-70. doi: 10.1016/j.acthis.2004.02.002.

Abstract

Juvenile and adult female flounder (Platichthys flesus (L.)) were caught either in the estuary of the most polluted European river, the Elbe, or as controls in a reference site to study pollution-induced xenobiotic resistance in their livers in relation to pathological alterations. In juvenile fish, livers displayed reversible and irreversible degenerative toxipathic lesion types but never showed (pre)neoplastic changes. Tumour frequencies up to 70% were found macroscopically in livers of adult female flounder which had progressed to adenomas and carcinomas in the most polluted site. Because male adult flounder show only up to 50% of livers containing early preneoplastic foci but never malignancies, we focussed our study on female individuals. (Pre)neoplastic changes ranged from early eosinophilic foci to basophilic foci, adenomas and hepatocellular carcinomas. Adenomas were generally eosinophilic whereas carcinomas were mainly basophilic. These phenotypical sequential changes strongly resemble those found in chemically-induced liver carcinogenesis in mammals. Characteristic mutations known from mammalian cancers have not been found so far in these flounder livers. Therefore, we investigated whether epigenetic events had induced a metabolic "resistant phenotype" of (pre)malignant cancer cells during hepatocellular carcinogenesis. With a quantitative immunohistochemical approach, we studied expression of P-glycoprotein (P-gp)-mediated multixenobiotic resistance (MXR), cytochrome P4501A1, glutathione-S-transferase-A which are key proteins in xenobiotic metabolism and elimination. Glucose-6-phosphate dehydrogenase (G6PDH) activity, the major source of the reducing power NADPH which is needed for biotransformation, oxyradical scavenging and biosynthesis, was detected as well. We observed upregulation of G6PDH activity already in early preneoplastic eosinophilic foci and subsequent further upregulation in basophilic foci and carcinomas. P-gp started to become overexpressed in basophilic foci and was overexpressed even more strongly in carcinomas and their invasively-growing protrusions (satellites). In carcinomas, P-gp protein was predominantly present in membranes of lysosomes which are the intracellular sites of deposition of xenobiotics. CYP450 was reduced whereas GST-A was increased in these carcinomas. Progression towards malignancy was positively correlated with levels of mitogenic organochlorines in these livers which are "fingerprint contaminants" of the river Elbe. We conclude that (pre)neoplastic hepatocytes in female flounder acquire growth advantages over normal hepatocytes by epigenetic metabolic adaptations during liver carcinogenesis as a result of chronic exposure to (pro)carcinogens in the polluted habitat.

摘要

幼年和成年雌性比目鱼(欧洲比目鱼,Platichthys flesus (L.))分别捕获于欧洲污染最严重的河流——易北河的河口,或作为对照捕获于一个参考地点,以研究其肝脏中污染诱导的异生物质抗性与病理变化的关系。在幼年比目鱼中,肝脏呈现出可逆和不可逆的退行性中毒性病变类型,但从未出现(癌)前病变。在污染最严重的地点,成年雌性比目鱼的肝脏中宏观上发现肿瘤发生率高达70%,这些肿瘤已发展为腺瘤和癌。由于成年雄性比目鱼只有高达50%的肝脏含有早期癌前病灶,但从未发生恶性肿瘤,因此我们将研究重点放在雌性个体上。(癌)前病变范围从早期嗜酸性病灶到嗜碱性病灶、腺瘤和肝细胞癌。腺瘤通常为嗜酸性,而癌主要为嗜碱性。这些表型的连续变化与哺乳动物化学诱导的肝癌发生过程中发现的变化非常相似。到目前为止,在这些比目鱼肝脏中尚未发现哺乳动物癌症中已知的特征性突变。因此,我们研究了表观遗传事件是否在肝细胞癌发生过程中诱导了(癌)前癌细胞的代谢“抗性表型”。通过定量免疫组织化学方法,我们研究了P-糖蛋白(P-gp)介导的多异生物质抗性(MXR)、细胞色素P4501A1、谷胱甘肽-S-转移酶-A的表达,这些都是异生物质代谢和消除中的关键蛋白。还检测了葡萄糖-6-磷酸脱氢酶(G6PDH)的活性,它是生物转化、氧自由基清除和生物合成所需的还原力NADPH的主要来源。我们观察到,早在癌前嗜酸性病灶中G6PDH活性就上调,随后在嗜碱性病灶和癌中进一步上调。P-gp在嗜碱性病灶中开始过度表达,在癌及其侵袭性生长的突起(卫星灶)中表达更强。在癌中,P-gp蛋白主要存在于溶酶体膜中,溶酶体是异生物质沉积的细胞内位点。在这些癌中,CYP450减少而GST-A增加。向恶性肿瘤的进展与这些肝脏中促有丝分裂有机氯的水平呈正相关,这些有机氯是易北河的“特征污染物”。我们得出结论,由于长期暴露于污染栖息地中的(前)致癌物,雌性比目鱼的(癌)前肝细胞在肝癌发生过程中通过表观遗传代谢适应获得了相对于正常肝细胞的生长优势。

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