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Table 1 Cancer pathway genes with significant upregulation after Acu and Rep stress, returning to normal after recovery

From: Stress alters the expression of cancer-related genes in the prostate

Gene ID/ Accesion

Gene name

Fold change

Con vs Acu

Fold change

Con vs Rep

Molecular function/biological process

Arnt P41739

Aryl hydrocarbon receptor nuclear translocator

1.51

1.23 (ns)

Transcription factor/response to hypoxia

Ets2 D4AAH4

V-ets erythroblastosis virus E26 oncogene homolog 2 (avian)

1.83

1.93

Transcription factor/cell differentiation

Krt14 Q6IFV1

Keratin 14

2.27

2.27

Cytoskeleton/maintenance of cell morphology

Serpinb2 P29524

Serpin peptidase inhibitor, clade B (ovalbumin), member 2

1.97

1.99

Endopeptidase inhibitor/apoptosis

Skp2 B2GUZ0

S-phase kinase-associated protein 2 (p45)

1.56

1.67

Ubiquitin ligase/cell cycle regulation

Slc2a1 P11167

Solute carrier family 2 (facilitated glucose transporter, member 1

1.25

1.32

Glucose transporter/metabolism (nutrient uptake)

Tinf2 Q5XIB8

TERF 1 (TRF1)- interacting nuclear factor 2

4.29

6.11

Telomeric DNA binding/chrosomome stability

  1. Italicized text denotes a gene that was only upregulated with Acu (but not Rep) stress, as indicated by “ns”; bold text denotes genes identified as proto-oncogenes. Accession numbers and molecular function/biological process obtained from UniProtKB database