首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Growth, microvessel density and tumor cell invasion of human colon adenocarcinoma under repeated treatment with hyperthermia and serotonin.
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Growth, microvessel density and tumor cell invasion of human colon adenocarcinoma under repeated treatment with hyperthermia and serotonin.

机译:在高温和5-羟色胺重复治疗下人结肠腺癌的生长,微血管密度和肿瘤细胞侵袭。

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The intratumoral microvessel density of malignant breast cancer has been shown to be an important prognostic marker. In this study, we tested whether repeated treatment with hyperthermia and serotonin (5-hydroxytryptamine) reduces tumor growth and alters tumor histology of a colon adenocarcinoma, and whether capillary density in this tumor can also be regarded as an important prognostic marker. Previously we have shown that acute treatment of colon adenocarcinoma with hyperthermia, alone or in combination with serotonin, selectively constricted tumor microvessels, which could reduce blood flow and inhibit tumor growth. Fourteen days after human colon adenocarcinoma had been transplanted under the dorsal epidermis of the ear of athymic nude mice, the surgically unprepared tumor-bearing ear of the sodium-pentobarbital-anesthetized animal was treated with hyperthermia alone (group 1, 43 degrees C for 45 min), or with hyperthermia plus topically applied serotonin (1 mM/l, 43 degrees C for 45 min, group 2) twice per week for 5 weeks. Control animals were not treated (group 3). Histological slides (stained with hematoxylin/eosin) were prepared 42 days after implantation, for analysis of tumor grading, tumor cell invasion into the surrounding tissue and microvessels, and the number of intratumoral microvessels. Repeated hyperthermia inhibited tumor growth, reduced the number of intratumoral microvessels, did not change tumor cell invasion and increased the necrotic area. Hyperthermia and serotonin did not influence tumor growth, but strongly reduced cell invasion and the number of microvessels. The area of necrosis was very large. Thus, analysis of microvessel density in colon adenocarcinoma seems not to be an important tool for predicting therapeutic efficacy.
机译:恶性乳腺癌的肿瘤内微血管密度已被证明是重要的预后指标。在这项研究中,我们测试了反复进行热疗和5-羟色胺(5-羟色胺)治疗是否会降低肿瘤的生长并改变结肠腺癌的肿瘤组织学,以及该肿瘤中的毛细血管密度是否也可以视为重要的预后指标。以前我们已经表明,单独或与5-羟色胺联合使用热疗对结肠腺癌进行急性治疗会选择性地收缩肿瘤微血管,从而减少血液流量并抑制肿瘤的生长。在将人结肠腺癌移植到无胸腺裸鼠的耳朵的背面表皮下十四天后,对未经手术准备的麻醉过的戊巴比妥钠麻醉的动物的耳朵进行单独的高温治疗(第1组,43摄氏度,45分钟),或伴有高热加局部应用5-羟色胺(1 mM / l,43摄氏度,45分钟,第2组),每周两次,共5周。对照动物未治疗(第3组)。植入后42天准备组织切片(用苏木精/曙红染色),用于分析肿瘤分级,肿瘤细胞侵袭周围组织和微血管以及肿瘤内微血管的数量。反复的高温抑制了肿瘤的生长,减少了肿瘤内微血管的数量,没有改变肿瘤细胞的侵袭并增加了坏死面积。热疗和5-羟色胺不会影响肿瘤的生长,但是会大大减少细胞侵袭和微血管的数量。坏死面积很大。因此,分析结肠腺癌中的微血管密度似乎并不是预测疗效的重要工具。

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