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Table 3 Results of studies that reported dysregulation of MEG8 in clinical samples

From: A review on the role of MEG8 lncRNA in human disorders

Tumor/ disorder type

Samples

Expression

(Tumor vs. Normal)

Kaplan-Meier analysis (impact of MEG8 up-regulation)

Univariate/ Multivariate cox regression

Association of MEG8 expression with Clinicopathologic characteristics

References

Lung cancer

21 pairs of NSCLC tissues and ANCTs

Up

–

–

–

[7]

37 pairs of NSCLC tissues and ANCTs

Up

–

–

–

[8]

Hepatocellular carcinoma

74 pairs of NSCLC tissues and ANCTs

Up

Lower OS and DFS

–

Edmondson Steiner grading, venous infiltration, and the number of tumor nodules

[11]

Bone-invasive pituitary adenomas

40 pituitary adenoma patients

Up

–

–

–

[12]

Ovarian cancer

GEO database: (GSE36668, GSE12470, GSE14407, and GSE27651), GEPIA2 and starBase database

Down

Better OS

–

–

[23]

Colorectal cancer

20 colorectal cancer, 20 adenomas, 20 healthy controls

Lower in colorectal cancer and adenomas than controls

–

–

–

[24]

Giant cell tumor of bone

5 GCTSCs and 5 MSCs

Down in GCTSCs

–

–

–

[25]

Diabetic nephropathy

66 DN patients 66 DM patients 66 healthy controls

Up in DN and DM than controls,

Up in DN than DM

–

–

–

[14]

Gestational diabetes mellitus

400 pregnant females (78 females were diagnosed as GDM during pregnancy)

Up in females who showed GDM

–

–

One month before

the diagnosis of GDM, plasma levels of MEG8 were sufficient to distinguish GDM patients from healthy controls.

GDM females with higher level of MEG8 showed higher incidence of kidney injury.

[26]

Trophoblast dysfunction and abortion

20 spontaneous abortion villi in early pregnancy and 20 normal early villi

Up in spontaneous abortion villi

–

–

–

[17]

Temple syndrome

3 Temple syndrome patients

DNA-hypermethylation of the MEG8-DMR was observed in 3 patients.

–

–

–

[27]

13 non-deletion TS14 patients

MEG8-DMR was hypermethylated in all patients.

–

–

–

[28]

Kagami-Ogata syndrome (KOS14)

4 KOS14 patients with different deletions

MEG8-DMR was hypomethylated in patients.

–

–

–

Osteoarthritis

22 OA patients and 22 healthy controls

Down

–

–

–

[19]

Abnormal semen

40 Semen samples from patients (8 normozoospermic, 16 asthenospermic, 3 oligospermic, 11 oligoasthenospermic and 2 morphologically deformed)

DMR of MEG8 were different in the abnormal semen groups.

MEG8 DMR methylation was significantly increased in the asthenospermic group.

Higher methylation levels of MEG8 DMR in the oligospermic and oligoasthenospermic groups were observed.

–

–

–

[29]

  1. ANCTs adjacent non-cancerous tissues, NSCLC non-small cell lung cancer, OS overall survival, DFS disease-free survival, GCTSCs neoplastic stromal, MSC mesenchymal stem cell, DN diabetic nephropathy, DM diabetes mellitus, GDM gestational diabetes mellitus, DMR differentially methylated region, TS14 Temple syndrome, OA Osteoarthritis