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通过薄膜原位酶谱法可在乳腺癌组织中检测到明胶酶活性的定位。

Localization of gelatinolytic activity can be detected in breast cancer tissues by film in situ zymography.

作者信息

Iwata H, Yamamoto M, Nemori R, Mizutani M, Iwase T, Miura S, Obata Y, Hara Y, Omoto Y, Toyama T, Yamashita H, Iwase H, Kobayashi S

机构信息

Department of Breast Surgery, Aichi Cancer Center hospital, 1-1 kanokoden, chikusa-ku, Nagoya 464-8681, Japan.

出版信息

Breast Cancer. 2001;8(2):111-5. doi: 10.1007/BF02967489.

Abstract

BACKGROUND

Extracellular matrix-degrading proteinases secreted by malignant tumor cells have been thought to play an essential role in the processes of invasion and metastasis. However, existence and localization of gelatinase activity in breast cancer tissues have not been clarified.

METHODS

We developed a novel film for highly reproducible detection and the localization of gelatinolytic activity. This film has a gelatin layer with a constant thickness 7 microm, and adequate crosslinking to control the speed of degradation by proteases. Cryosections of several breast cancer tissues were put on this gelatin film and incubated for 16 hrs at 37 degrees C. After staining with ponceau 3R dye, the digested area was evaluated under light microscopy.

RESULTS

Digestion of gelatin was detected in more than 90%of breast cancer specimens, although it varied in degree and area for each case. In most cases, the gelatinolytic activity was located within cancer nests, and was not detected in stromal cells surrounding cancer cells. The gelatinolytic activity was inhibited by 1,10-phenanthroline, an inhibitor of matrix metalloproteinases (MMPs).

CONCLUSIONS

In this study, the localization of net MMP activity was confirmed in breast cancer nest using film in situ zymography. Detailed analysis on the relationship between the strength or distribution of MMP activity and malignancy are anticipated in the future.

摘要

背景

恶性肿瘤细胞分泌的细胞外基质降解蛋白酶被认为在侵袭和转移过程中起重要作用。然而,乳腺癌组织中明胶酶活性的存在及定位尚未明确。

方法

我们开发了一种用于高度可重复检测和明胶酶活性定位的新型薄膜。该薄膜有一层厚度恒定为7微米的明胶层,并经过适当交联以控制蛋白酶降解的速度。将数个乳腺癌组织的冰冻切片置于该明胶薄膜上,于37℃孵育16小时。用丽春红3R染料染色后,在光学显微镜下评估消化区域。

结果

在90%以上的乳腺癌标本中检测到明胶消化,尽管每个病例的程度和区域有所不同。在大多数情况下,明胶酶活性位于癌巢内,在癌细胞周围的基质细胞中未检测到。明胶酶活性受到基质金属蛋白酶(MMPs)抑制剂1,10 - 菲咯啉的抑制。

结论

在本研究中,使用薄膜原位酶谱法在乳腺癌巢中证实了净MMP活性的定位。未来有望对MMP活性的强度或分布与恶性程度之间的关系进行详细分析。

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