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使用金簇对肿瘤细胞侵袭进行定性和定量分析。

Qualitative and Quantitative Analysis of Tumor Cell Invasion Using Au Clusters.

作者信息

Zhang Xiangchun, Zheng Qinqin, Wang Ziqi, Xu Chao, Han Haolei, Li Aiping, Ma Guicen, Li Jiaojiao, Lu Chengyin, Chen Hongping, Zhang Zhichao

机构信息

Tea Research Institute, Chinese Academy of Agricultural Sciences, Hangzhou 310008, China.

College of Chemistry and Material Science, Shandong Agricultural University, Taian 271018, China.

出版信息

Nanomaterials (Basel). 2021 Dec 31;12(1):145. doi: 10.3390/nano12010145.

Abstract

Tumor invasion/metastasis is still the major cause of death in cancer patients. Membrane type-1 matrix metalloproteinase (MT1-MMP) is directly related to tumor invasion/metastasis. To accurately and quickly distinguish the risk of invasion/metastasis of primary tumor cells, it is urgent to develop a simple and precise quantitative method to distinguish the expression level of MT1-MMP. In this work, we have constructed red fluorescent Au clusters with peroxidase-like properties that could specifically bind to MT1-MMP on human cervical cancer cells. After MT1-MMP was labelled with Au clusters, we could visually see red fluorescence of MT1-MMP on cervical cancer cells via fluorescence microscopy and catalytic color imaging using an ordinary optical microscope. The constructed Au clusters contained 26 Au atoms; thus, the amount of MT1-MMP on cervical cancer cells could be accurately quantified using inductively coupled plasma mass spectrometry (ICP-MS). More importantly, the invasion/metastasis capabilities of the cervical cancer Siha, Caski and Hela cells with different MT1-MMP amounts could be accurately distinguished by fluorescence/catalysis qualitative imaging and ICP-MS quantitative analysis. This method of qualitative/quantitative analysis of tumor-associated proteins on cancer cells has great potential for accurately diagnosing aggressive tumor cells and assessment of their invasion/metastasis risk.

摘要

肿瘤侵袭/转移仍然是癌症患者死亡的主要原因。膜型-1基质金属蛋白酶(MT1-MMP)与肿瘤侵袭/转移直接相关。为了准确、快速地区分原发性肿瘤细胞侵袭/转移的风险,迫切需要开发一种简单而精确的定量方法来区分MT1-MMP的表达水平。在这项工作中,我们构建了具有过氧化物酶样性质的红色荧光金簇,其能够特异性结合人宫颈癌细胞上的MT1-MMP。在用金簇标记MT1-MMP后,我们可以通过荧光显微镜以及使用普通光学显微镜的催化彩色成像直观地看到宫颈癌细胞上MT1-MMP的红色荧光。所构建的金簇包含26个金原子;因此,可以使用电感耦合等离子体质谱(ICP-MS)准确量化宫颈癌细胞上MT1-MMP的量。更重要的是,通过荧光/催化定性成像和ICP-MS定量分析,可以准确区分具有不同MT1-MMP量的宫颈癌Siha、Caski和Hela细胞的侵袭/转移能力。这种对癌细胞上肿瘤相关蛋白进行定性/定量分析的方法在准确诊断侵袭性肿瘤细胞及其侵袭/转移风险评估方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232b/8746878/3b369a3b7ef2/nanomaterials-12-00145-sch001.jpg

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