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疏水分级分离增强了通过质谱法检测三阴性乳腺癌中的新型蛋白质。

Hydrophobic Fractionation Enhances Novel Protein Detection by Mass Spectrometry in Triple Negative Breast Cancer.

作者信息

Lu Ming, Whitelegge Julian P, Whelan Stephen A, He Jianbo, Saxton Romaine E, Faull Kym F, Chang Helena R

机构信息

Gonda/UCLA Breast Cancer Research Laboratory, David Geffen School of Medicine, Los Angeles, California.

出版信息

J Proteomics Bioinform. 2010 Jan 22;3(2):1-10. doi: 10.4172/jpb.1000118.

Abstract

It is widely believed that discovery of specific, sensitive and reliable tumor biomarkers can improve the treatment of cancer. The goal of this study was to develop a novel fractionation protocol targeting hydrophobic proteins as possible cancer cell membrane biomarkers. Hydrophobic proteins of breast cancer tissues and cell lines were enriched by polymeric reverse phase columns. The retained proteins were eluted and digested for peptide identification by nano-liquid chromatography with tandem mass spectrometry using a hybrid linear ion-trap Orbitrap.Hundreds of proteins were identified from each of these three specimens: tumors, normal breast tissue, and breast cancer cell lines. Many of the identified proteins defined key cellular functions. Protein profiles of cancer and normal tissues from the same patient were systematically examined and compared. Stem cell markers were overexpressed in triple negative breast cancer (TNBC) compared with non-TNBC samples. Because breast cancer stem cells are known to be resistant to radiation and chemotherapy, and can be the source of metastasis frequently seen in patients with TNBC, our study may provide evidence of molecules promoting the aggressiveness of TNBC.The initial results obtained using a combination of hydrophobic fractionation and nano-LC mass spectrometry analysis of these proteins appear promising in the discovery of potential cancer biomarkers. When sufficiently refined, this approach may prove useful for early detection and better treatment of breast cancer.

摘要

人们普遍认为,发现特异性、敏感性和可靠性高的肿瘤生物标志物可以改善癌症治疗。本研究的目的是开发一种新的分级分离方案,以富集疏水蛋白作为潜在的癌细胞膜生物标志物。通过聚合物反相柱富集乳腺癌组织和细胞系中的疏水蛋白。洗脱保留的蛋白质并进行消化,然后使用混合线性离子阱-轨道阱通过纳升液相色谱-串联质谱法进行肽段鉴定。从肿瘤、正常乳腺组织和乳腺癌细胞系这三个样本中分别鉴定出了数百种蛋白质。许多已鉴定的蛋白质具有关键的细胞功能。系统地检查和比较了同一患者癌症组织和正常组织的蛋白质谱。与非三阴性乳腺癌(TNBC)样本相比,干细胞标志物在三阴性乳腺癌中过表达。由于已知乳腺癌干细胞对放疗和化疗具有抗性,并且可能是TNBC患者常见转移的来源,我们的研究可能为促进TNBC侵袭性的分子提供证据。使用疏水分级分离和纳米液相色谱-质谱联用分析这些蛋白质获得的初步结果,在发现潜在癌症生物标志物方面似乎很有前景。经过充分完善后,这种方法可能对乳腺癌的早期检测和更好治疗有用。

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