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Establishment of metastatic liver carcinoma model by implanting AX7 cells into rabbit liver, and its histological findings

机译:AX7细胞植入兔肝转移肝癌模型的建立及其组织学发现

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摘要

Background: Progression of metastatic liver carcinoma from any original cancer is aggressive and the prognosis is very poor. Therefore the new model that is easily approachable to study the propagation and prognosis of metastatic liver carcinoma is necessary. The aim of this study is to confirm the tumor formation and metastatic activity of anaplastic thyroid cancer and to support the research basis for the next generation cancer treatment that is to be developed, by carrying out additional experiments like cytokine stimulation. We investigated sequential findings of immunohistochemistry of rabbit hepatic malignancy induced by AX7 cells.Methods: 13 rabbits implanted with AX7 cells directly into liver parenchyme with laparotomy were investigated by histopathology examination, immunohistochemistry, which is useful for the evaluation of metastatic cancer angiogenesis. Growing tissue at the edge of the mass was collected and placed in the petri dish filled with saline. After removing necrotic and fibrous tissue, tumor tissue was cut into pieces, placed in saline, and extracted during the experiment.Results: Tumor growth and malignancy was confirmed on the 10th day after AX7 cells were implanted into liver. Positive for VEGF staining was found in the cytoplasm or cell membrane. The scores for VEGF stained cells were moderately positive (++) on day 10, strongly positive (+++) on day 44. Ki-67-positive hepatocytes reached at 65% on day 10, at 65.78% on day 14, at 66.4% on day 30, at 67.88% on day 44.Conclusion: AX7 cells implanted into liver can be used as a new rabbit metastatic liver carcinoma model and would become useful for human metastatic liver carcinoma studies. Future studies may facilitate the establishment of an effective systemic therapy for the metastatic liver cancer.
机译:背景:转移性肝癌从任何原始癌的进展都具有侵略性,预后很差。因此,有必要建立一种易于研究转移性肝癌的传播和预后的新模型。这项研究的目的是通过进行其他实验(如细胞因子刺激)来确认间变性甲状腺癌的肿瘤形成和转移活性,并为即将开发的下一代癌症治疗提供研究基础。我们研究了AX7细胞诱导的兔肝恶性肿瘤免疫组织化学的顺序发现。方法:对13只将AX7细胞直接植入肝实质并行剖腹术的兔子进行了组织病理学检查,免疫组织化学研究,这对评估其有效性是有帮助的。转移性肿瘤血管生成。收集在肿块边缘的生长组织,并将其置于充满盐水的培养皿中。在切除坏死和纤维组织后,将肿瘤组织切成薄片,放入盐水中,然后在实验过程中提取。结果:在将AX7细胞植入肝脏后的第10天确认了肿瘤的生长和恶性。在细胞质或细胞膜中发现VEGF染色阳性。 VEGF染色的细胞在第10天的得分为中度阳性(++),在第44天的得分为强阳性(+++)。Ki-67阳性肝细胞在第10天达到65%,在第14天达到65.78%。第30天为66.4%,第44天为67.88%。结论:植入肝脏的AX7细胞可以用作新的兔转移性肝癌模型,并将对人类转移性肝癌研究有用。未来的研究可能有助于建立有效的全身治疗转移性肝癌的方法。

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