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钴胺素转运蛋白、细胞表面受体和Ki-67在自然发生的犬猫恶性肿瘤及相邻正常组织中的免疫组织化学定量分析。

Immunohistochemical quantification of the cobalamin transport protein, cell surface receptor and Ki-67 in naturally occurring canine and feline malignant tumors and in adjacent normal tissues.

作者信息

Sysel Annette M, Valli Victor E, Bauer Joseph A

机构信息

Bauer Research Foundation, Akron, Ohio, USA.

VDx Veterinary Pathology Services, Davis, California, USA.

出版信息

Oncotarget. 2015 Feb 10;6(4):2331-48. doi: 10.18632/oncotarget.3206.

Abstract

Cancer cells have an obligate need for cobalamin (vitamin B12) to enable DNA synthesis necessary for cellular replication. This study quantified the immunohistochemical expression of the cobalamin transport protein (transcobalamin II; TCII), cell surface receptor (transcobalamin II-R; TCII-R) and proliferation protein (Ki-67) in naturally occurring canine and feline malignant tumors, and compared these results to expression in corresponding adjacent normal tissues. All malignant tumor tissues stained positively for TCII, TCII-R and Ki-67 proteins; expression varied both within and between tumor types. Expression of TCII, TCII-R and Ki-67 was significantly higher in malignant tumor tissues than in corresponding adjacent normal tissues in both species. There was a strong correlation between TCII and TCII-R expression, and a modest correlation between TCII-R and Ki-67 expression in both species; a modest association between TCII and Ki-67 expression was present in canine tissues only. These results demonstrate a quantifiable, synchronous up-regulation of TCII and TCII-R expression by proliferating canine and feline malignant tumors. The potential to utilize these proteins as biomarkers to identify neoplastic tissues, streamline therapeutic options, evaluate response to anti-tumor therapy and monitor for recurrent disease has important implications in the advancement of cancer management for both human and companion animal patients.

摘要

癌细胞对钴胺素(维生素B12)有绝对需求,以实现细胞复制所必需的DNA合成。本研究对自然发生的犬猫恶性肿瘤中钴胺素转运蛋白(转钴胺素II;TCII)、细胞表面受体(转钴胺素II受体;TCII-R)和增殖蛋白(Ki-67)的免疫组化表达进行了定量,并将这些结果与相应相邻正常组织中的表达进行了比较。所有恶性肿瘤组织中TCII、TCII-R和Ki-67蛋白均呈阳性染色;表达在肿瘤类型内和肿瘤类型间均有差异。在两个物种中,恶性肿瘤组织中TCII、TCII-R和Ki-67的表达均显著高于相应的相邻正常组织。在两个物种中,TCII和TCII-R表达之间存在强相关性,TCII-R和Ki-67表达之间存在适度相关性;仅在犬组织中,TCII和Ki-67表达之间存在适度关联。这些结果表明,增殖的犬猫恶性肿瘤可使TCII和TCII-R表达出现可量化的同步上调。利用这些蛋白作为生物标志物来识别肿瘤组织、简化治疗选择、评估抗肿瘤治疗反应以及监测疾病复发的潜力,对人类和伴侣动物患者癌症管理的进展具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144b/4385855/2fdf02140868/oncotarget-06-2331-g001a.jpg

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