Knockdown of NLE1 inhibits development of malignant melanoma in vitro and in vivo NLE1 promotes development of malignant melanoma
Journal Article
·
· Experimental Cell Research
- Department of Orthopedics, Shengjing Hospital of China Medical University, 36 Sanhao Street, Heping District, Shenyang, Liaoning, 110004 (China)
- Department of Rehabiliation, Shengjing Hospital of China Medical University, 36 Sanhao Street, Heping District, Shenyang, Liaoning, 110004 (China)
Melanoma, which originates from neural crest derived melanocytes, causes severe pain and even death to numerous patients. Previous studies reported that Notchless Homolog 1 (NLE1) plays an important role in cell proliferation, transcription and signal transduction. However, the clinical significance and biological behavior of NLE1 in melanoma remain a mystery. Thus, the role of NLE1 in melanoma was investigated in vitro and in vivo. The expression of NLE1 in melanoma was elevated and the expression level was positively correlated with lymphatic metastasis and tumor stage. In addition, NLE1 knockdown by shRNA specifically inhibited proliferation, enhanced the apoptotic sensitivity and hindered migration of melanoma cells in vitro. Mice xenograft model further showed that NLE1 knockdown could inhibit the tumor formation of melanoma in vivo. Additionally, the induction of apoptosis of melanoma cells by NLE1 knockdown required the participation of a series of apoptosis-related proteins. Besides, NLE1 can activate the PI3K/AKT signaling pathway. In summary, NLE1 was involved in the development and progression of melanoma, which may be a novel potential target for molecular therapy of melanoma.
- OSTI ID:
- 23195607
- Journal Information:
- Experimental Cell Research, Journal Name: Experimental Cell Research Journal Issue: 2 Vol. 404; ISSN 0014-4827; ISSN ECREAL
- Country of Publication:
- United States
- Language:
- English
Similar Records
EIF3H knockdown inhibits malignant melanoma through regulating cell proliferation, apoptosis and cell cycle
CXCL5 knockdown expression inhibits human bladder cancer T24 cells proliferation and migration
NFAT5 promotes in vivo development of murine melanoma metastasis
Journal Article
·
Sat May 15 00:00:00 EDT 2021
· Experimental Cell Research
·
OSTI ID:23195309
CXCL5 knockdown expression inhibits human bladder cancer T24 cells proliferation and migration
Journal Article
·
Fri Mar 28 00:00:00 EDT 2014
· Biochemical and Biophysical Research Communications
·
OSTI ID:22416320
NFAT5 promotes in vivo development of murine melanoma metastasis
Journal Article
·
Wed Nov 14 23:00:00 EST 2018
· Biochemical and Biophysical Research Communications
·
OSTI ID:23107764