Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P42345 (
mTOR
)
26,049
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Lung cancer is the leading cause of cancer-related mortality worldwide.
PEST-containing nuclear protein
(
PCNP
) has been found in the nucleus of cancer cells. Whether
PCNP
plays a role in the growth of lung adenocarcinoma is still unknown. In the present study, the results indicated that the level of
PCNP
in lung adenocarcinoma tissue was significantly higher than that in corresponding adjacent non-tumor tissue. Over-expression of
PCNP
promoted the proliferation, migration, and invasion of lung adenocarcinoma cells, while down-regulation of
PCNP
exhibited opposite effects.
PCNP
over-expression decreased apoptosis through up-regulating the expression levels of phospho (p)-signal transducers and activators of transcription (STAT) 3 and p-STAT5 in lung adenocarcinoma cells, whereas
PCNP
knockdown showed opposite trends.
PCNP
overexpression enhanced autophagy by increasing the expression levels of p-phosphatidylinositol 3-kinase (PI3K), p-Akt, and p-
mammalian target of rapamycin
(
mTOR
) in lung adenocarcinoma cells, however an opposite trend was observed in the sh-
PCNP
group. In addition, overexpression of
PCNP
showed the tumor-promoting effect on xenografted lung adenocarcinoma, while
PCNP
knockdown reduced the growth of lung adenocarcinoma via regulating angiogenesis. Our study elucidates that
PCNP
can regulate the procession of human lung adenocarcinoma cells via STAT3/5 and PI3K/Akt/
mTOR
signaling pathways.
PCNP
may be considered as a promising biomarker for the diagnosis and prognosis in patients with lung adenocarcinoma. Furthermore,
PCNP
can be a novel therapeutic target and potent
PCNP
inhibitors can be designed and developed in the treatment of lung adenocarcinoma.
...
PMID:PEST-containing nuclear protein regulates cell proliferation, migration, and invasion in lung adenocarcinoma. 3087 82