在三阴性乳腺癌中,含 TBC1 结构域的蛋白质经常与糖酵解表型的诱导有关。

IF 8.1 1区 生物学 Q1 CELL BIOLOGY Cell Death & Disease Pub Date : 2024-09-04 DOI:10.1038/s41419-024-07037-2
Mariadomenica Lupi, Daniele Avanzato, Stefano Confalonieri, Flavia Martino, Rosa Pennisi, Emanuela Pupo, Valentina Audrito, Stefano Freddi, Giovanni Bertalot, Francesca Montani, Bronislava Matoskova, Sara Sigismund, Pier Paolo Di Fiore, Letizia Lanzetti
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引用次数: 0

摘要

代谢可塑性是癌症的一个特征,而代谢改变是一个很有希望的治疗靶点。由于细胞代谢在多个水平上受膜交通的控制,我们研究了含 TBC1 结构域的蛋白(TBC1Ds)参与癌症代谢调控的情况。这些蛋白的特点是存在一个 RAB-GAP 结构域,即 TBC1 结构域,通常作为膜交通的主开关 RAB 的衰减器发挥作用。然而,一些 TBC1D 的催化残基发生了突变,预示其生物学功能与直接调节 RAB 活性不同。在此,我们报告了几个编码TBC1Ds的基因在三阴性乳腺癌(TNBC)中的表达水平高于其他亚型乳腺癌(BC),并能预测预后。正交转录组学/代谢组学分析表明,预后TBC1Ds的表达与BC细胞系中糖酵解代谢的升高有关。对之前分析中的三个热点(TBC1D31、TBC1D22B 和 TBC1D7)进行深入研究后发现,它们的表达升高是决定 TNBC 细胞系中糖酵解表型的因果关系。我们进一步发现,TBC1D7 对 BC 细胞糖代谢的影响与已知的参与 TSC1/TSC2 复合物以及随之而来的 mTORC1 活性下调无关。由于TBC1D7在TNBC中表现为一个独立的预后生物标志物,因此它可用于区分预后良好的患者和预后不良的患者,前者可免于接受积极的治疗,后者则可能受益于抗糖酵解靶向疗法。总之,我们的研究结果凸显了TBC1D如何将TNBC的疾病侵袭性与代谢改变联系在一起。鉴于这种BC亚型的高度异质性,TBC1Ds可能是预测预后和指导治疗决策的重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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TBC1 domain-containing proteins are frequently involved in triple-negative breast cancers in connection with the induction of a glycolytic phenotype.

Metabolic plasticity is a hallmark of cancer, and metabolic alterations represent a promising therapeutic target. Since cellular metabolism is controlled by membrane traffic at multiple levels, we investigated the involvement of TBC1 domain-containing proteins (TBC1Ds) in the regulation of cancer metabolism. These proteins are characterized by the presence of a RAB-GAP domain, the TBC1 domain, and typically function as attenuators of RABs, the master switches of membrane traffic. However, a number of TBC1Ds harbor mutations in their catalytic residues, predicting biological functions different from direct regulation of RAB activities. Herein, we report that several genes encoding for TBC1Ds are expressed at higher levels in triple-negative breast cancers (TNBC) vs. other subtypes of breast cancers (BC), and predict prognosis. Orthogonal transcriptomics/metabolomics analysis revealed that the expression of prognostic TBC1Ds correlates with elevated glycolytic metabolism in BC cell lines. In-depth investigations of the three top hits from the previous analyses (TBC1D31, TBC1D22B and TBC1D7) revealed that their elevated expression is causal in determining a glycolytic phenotype in TNBC cell lines. We further showed that the impact of TBC1D7 on glycolytic metabolism of BC cells is independent of its known participation in the TSC1/TSC2 complex and consequent downregulation of mTORC1 activity. Since TBC1D7 behaves as an independent prognostic biomarker in TNBC, it could be used to distinguish good prognosis patients who could be spared aggressive therapy from those with a poor prognosis who might benefit from anti-glycolytic targeted therapies. Together, our results highlight how TBC1Ds connect disease aggressiveness with metabolic alterations in TNBC. Given the high level of heterogeneity among this BC subtype, TBC1Ds could represent important tools in predicting prognosis and guiding therapy decision-making.

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来源期刊
Cell Death & Disease
Cell Death & Disease CELL BIOLOGY-
CiteScore
15.10
自引率
2.20%
发文量
935
审稿时长
2 months
期刊介绍: Brought to readers by the editorial team of Cell Death & Differentiation, Cell Death & Disease is an online peer-reviewed journal specializing in translational cell death research. It covers a wide range of topics in experimental and internal medicine, including cancer, immunity, neuroscience, and now cancer metabolism. Cell Death & Disease seeks to encompass the breadth of translational implications of cell death, and topics of particular concentration will include, but are not limited to, the following: Experimental medicine Cancer Immunity Internal medicine Neuroscience Cancer metabolism
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