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. 2020 Sep 23;21(19):6995. doi: 10.3390/ijms21196995

Table 1.

In vivo expression of different IGF1 isoforms (mRNA, protein) in selected human cancers.

Human Cancer Tissue Material/Technique IGF1 mRNAs IGF1 Propeptides/Peptides No of ref.
IGF1Ea (Class I and II) IGF1Eb (Class I and II) IGF1Ec (Class I and II) Pro-Ea/Ea Pro-Eb/Eb Pro-Ec/Ec (MGF)
Brain cancer n = 9 gliomas; IHC, RT-PCR (+) (+) (-) nt [183]
Colorectal cancer One colonic and one retro-sigmoidal NENs; IHC nt nt (-) Ec peptide in both CRC [32]
n = 13 pairs of CRC/CT; IHC; qRT-PCR (+) ↑ vs. CT; ↑ vs. Eb&Ec; (+) ↓ vs. CT; ↑ vs. Ec (+) ≈ vs. CT nt [104]
↓ class I/II vs. CT; ↑ class II vs. class I;
n = 28 pairs of CRC/CT; IHC; qRT-PCR (+); 82% of all transcripts; ≈ vs. Eb; ↑ vs. Ec (+); 17% of all transcripts; ↑ vs. Ec (+); ~1% of all transcripts nt [105]
↓ all isoforms vs. CT; CRC: Class I - 59%; class II - 41%, in quantitative expression - NS
CRC/polyps/CT; fluorescent gold nanoparticles nt nt (+) Ec peptide (MGF); in C [34]
Epithelial Cervical cancer One uterine cervical NEN; IHC nt nt (+) Ec peptide; in C [32]
n = 29 squamous CC (HPV+), n = 28 L-SIL (HPV+), n = 30 H-SIL (HPV+), n = 20 CT (HPV-); PCR, qRT-PCR (+++) 85% in CC; 92% in CT (+++) 14% in CC; 8% in CT (+++) 1% in CC and CT nt [49]
Class I - 69–86%; class II - 14–31%; ↑ of all isoforms in pre-cancerous tissues vs. CC and CT, and a shift in the balance towards IGF1Eb in CC; (+) correlation between the FOX2 mRNA expression and Ea/Eb in precancerous and CC, and Ec in L-SIL and H-SIL
Gastric cancer n = 8 NENs; IHC nt nt (+) Ec peptide in 37.5%; in C [32]
Lung cancer n = 2 NENs; IHC nt nt (+) Ec peptide in one LC; in C [32]
Pancreatic cancer n = 17 NENs; IHC nt nt (+) Ec peptide in 58.8%; in C [32]
Prostate cancer IHC, Western blot, RT-PCR nt nt (+++) MGF; ↑ PC and PIN vs. CT [108]
n = 83 patients; paraffin sections; IHC nt nt (+) Ec peptide; in C; #, ↑ Ec peptide [109]
n = 78 patients; IHC; Western blot, qRT-PCR nt nt (+) Ec peptide; #, ↑ Ec peptide [166]
Small intestine cancer n = 9 NENs, IHC nt nt (+) Ec in 44.4%; in C [32]
Thyroid cancer n = 92 of different types of TC; IHC, qRT-PCR nt (+) IGF1Ec; ↑in more aggressive vs. non-aggressive papillary TC nt (+) Ec peptide in papillary TC; in C; #, ↑ Ec [35]
Urinary bladder cancer n = 46 biopsies/CT; qRT-PCR (+) marginally ↑ vs. CT (+) marginally ↑ vs. CT ↓ vs. CT; #, ↓IGF1Ec nt nt [33]
↑ of all IGF1 mRNA isoforms in in situ carcinomas
UPO n = 4 NENs; IHC nt nt (+) Ec peptide in 100%; in C [32]
Others NENs; appendiceal (n = 3), gallbladder (n = 1); IHC nt nt (-) Ec peptide in 100% [32]

Legend: (+)—positive expression; (+++)—overexpression; (-)—lack of expression; ↑/↓—significant increased/decreased; #—significant correlation with clinical TNM stage, tumor grade, and/or disease recurrence; C—cytoplasm; CC—cervical cancer; CRC—colorectal cancer; CT—control tissue; HPV—Human Papillomavirus; H-SIL—high-grade squamous intraepithelial lesions; IHC—immunohistochemistry; L-SIL—low-grade squamous intraepithelial lesions; MGF—mechano-growth factor; NENs—neuroendocrine neoplasms; NS—non significant; nt—non tested; PC—prostate cancer; PIN—prostatic intraepithelial neoplasia; qRT-PCR—quantitative real-time polymerase chain reaction (PCR); TC—thyroid cancer; UPO—cancers of unknown primary origin.