[1] PubMed ID: | 32871048 |
Disease Name: | lung squamous cell carcinoma |
Sample: | LUSC samples,LUSC cells |
Dysfunction Pattern: | regulation[stabilizing HMGB3 by TAF15] |
Validated Method: | RNA Pull-Down//Western Blot//Tunel//Flow Cytometry//qRT-PCR//FISH//Luciferase Report Assay//Colony Formation Assay//EdU Staining//Transwell Assay |
Description: | Through online database GEPIA, lncRNA PITPNA antisense RNA 1 (PITPNA-AS1) was highly expressed in LUSC samples, and these tendency was further affirmed in LUSC cells. All in all, PITPNA-AS1 promoted the proliferation and migration of LUSC cells via stabilizing HMGB3 by TAF15. |
Causality: | Yes |
Causal Description: | Functional experiments verified that depletion of PITPNA-AS1 hampered the proliferative and migratory abilities, but accelerated apoptosis of LUSC cells. |
Clinical-realted Application: | |
[2] PubMed ID: | 35588441 |
Disease Name: | lung squamous cell carcinoma |
Sample: | LUSC tissues and cells |
Dysfunction Pattern: | Interaction(LncRNA PITPNA-AS1/miR-223-3p/PTN axis ) |
Validated Method: | RNA Pull-Down//Western Blot//Transfection//CCK8//qRT-PCR//Luciferase Report Assay// In Vivo Experiment//Colony Formation Assay//Transwell Assay |
Description: | The lncRNA PITPNA-AS1 had increased expression in LUSC and was linked to a poor prognosis. This mechanistic investigation showed that PITPNA-AS1 absorbed miR-223-3p and that miR-223-3p targeted PTN. MiR-223-3p inhibition or PTN overexpression might reverse the inhibitory effects of PITPNA-AS1 suppression on LUSC progression, as demonstrated by rescue experiments. In addition, the PITPNA-AS1/miR-223-3p/PTN axis accelerated tumor development in vivo. |
Causality: | Yes |
Causal Description: | In LUSC, PITPNA-AS1 also enhanced cell proliferation, migration, invasion, and stemness. |
Clinical-realted Application: | The lncRNA PITPNA-AS1 had increased expression in LUSC and was linked to a poor prognosis. |
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