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. 2019 Oct 28;8(11):1330. doi: 10.3390/cells8111330

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© 2019 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Differentially expressed protein synthesis and degradation-, epigenetic regulation, DNA structure-, and DNA replication-related proteins following short- and long-term treatments with si-VDAC1 or si-NT. Quantitative analysis of the LC-HR MS/MS data. Differentially expressed proteins of mouse (A) and human (B) origin associated with the microenvironment in tumors treated with si-hVDAC1 for short and long periods, are presented as fold change of the expression in si-VDAC1-TTs, relative to si-NT-TTs. (■) and () indicate short-term and long-term treatment with si-hVDAC1, respectively. * p ≤ 0.05, ** p ≤ 0.01.

Inline graphic — Differentially expressed protein synthesis and degradation-, epigenetic regulation, DNA structure-, and DNA replication-related proteins following short- and long-term treatments with si-VDAC1 or si-NT. Quantitative analysis of the LC-HR MS/MS data. Differentially expressed proteins of mouse (A) and human (B) origin associated with the microenvironment in tumors treated with si-hVDAC1 for short and long periods, are presented as fold change of the expression in si-VDAC1-TTs, relative to si-NT-TTs. (■) and () indicate short-term and long-term treatment with si-hVDAC1, respectively. * p ≤ 0.05, ** p ≤ 0.01.