Exploration of Digestive Diseases

From: Liver metastatic colonization by invasive cancer cells: a review of potential biomarkers with mitochondrial involvement

Table 1. List of potential mitochondrial biomarkers involved in liver metastases by MPM invasive cells

Gene	Full name	Change #
Slc25a5	ADP/ATP translocase 2	↓
Prdx5	Peroxiredoxin-5, mitochondrial	↓
Acadm	Medium-chain specific acyl-CoA dehydrogenase, mitochondrial	↓
Acads	Short-chain specific acyl-CoA dehydrogenase, mitochondrial	↓
Hmgcs2	Hydroxymethylglutaryl-CoA synthase, mitochondrial	↓
Idh3a	Isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial	↓
Dlat	Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial	↓
Cpox	Oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial	↓
Ndufa10	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial	↓
Aldh5a1	Succinate-semialdehyde dehydrogenase, mitochondrial	↓
Fis1	Mitochondrial fission 1 protein	↓
Sardh	Sarcosine dehydrogenase, mitochondrial	↓
Nln	Neurolysin, mitochondrial	↓
Acadl	Long-chain specific acyl-CoA dehydrogenase, mitochondrial	↑
Aco2	Aconitate hydratase, mitochondrial	↑
Hadha	Trifunctional enzyme subunit alpha, mitochondrial	↑
Grpel1	GrpE protein homolog 1, mitochondrial	↑
Micu1	Calcium uptake protein 1, mitochondrial	↑
Uqcrq	Cytochrome b-c1 complex subunit 8	↑
Vdac2	Voltage-dependent anion-selective channel protein 2	↑
Ogdh	2-oxoglutarate dehydrogenase, mitochondrial	↑
Phb	Prohibitin	↑
Mgst1*	Microsomal glutathione S-transferase 1	↑
Decr1*	2,4-dienoyl-CoA reductase 1	↓
Prdx3*	Thioredoxin-dependent peroxide reductase, mitochondrial	↓

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* Proteins not strictly located in the mitochondria (according to https://www.proteinatlas.org/). Gene names are given for Rattus norvegicus (according to https://www.uniprot.org/). #: significant changes (P < 0.05) in G2 vs. G1, and G3 vs. G2. ↑: increase; ↓: decrease

Note. Adapted from “Curcumin treatment identifies therapeutic targets within biomarkers of liver colonization by highly invasive mesothelioma cells—potential links with sarcomas,” by Pouliquen DL, Boissard A, Henry C, Blandin S, Richomme P, Coqueret O, et al. Cancers (Basel). 2020;12:3384 (https://www.mdpi.com/2072-6694/12/11/3384). CC BY.

Declarations

Author contributions

DLP: Writing—original draft, Writing—review & editing.

Conflicts of interest

The author declares that he has no conflicts of interest.

Ethical approval

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Availability of data and materials

Not applicable.

Funding

This review was prepared with the support of the University of Angers, including the Mir program “Mobilité Internationale pour la Recherche” between the Universities of Angers (France) and Turin (Italy) in 2020–2021 and 2021–2022. The funder (University of Angers) had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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