Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancer
Abstract Micro-RNAs (mi-RNAs) can regulate various tumor suppressor genes or oncogenes thus they were monitored in various types of cell carcinoma. Lung cancer extensive progress has led not only to understanding the molecular pathways governing human lung cancer, but it has also created a vast rese...
Saved in:
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2025-06-01
|
| Series: | Cancer Nanotechnology |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s12645-025-00331-4 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1849329028231593984 |
|---|---|
| author | Mai O. Kadry Rehab M. Abdel-Megeed |
| author_facet | Mai O. Kadry Rehab M. Abdel-Megeed |
| author_sort | Mai O. Kadry |
| collection | DOAJ |
| description | Abstract Micro-RNAs (mi-RNAs) can regulate various tumor suppressor genes or oncogenes thus they were monitored in various types of cell carcinoma. Lung cancer extensive progress has led not only to understanding the molecular pathways governing human lung cancer, but it has also created a vast reservoir for alternative development of novel liposomal Nano-medicines counteracting this malignancy. Liposomal drug delivery system can passively accrue in cancer cells via the retention phenomenon and enhanced permeability. This article highlighted liposomal-loaded nano-medicine as a potential treatment for lung cancer and clarifies the correlated miRNA and mRNA gene profile. Lung cancer was induced experimentally in rats via 3-methylcholanthrene (3-MCA) in a dose of 40 mg IV for 4 months followed by treatment via certain liposomal-loaded compounds, namely, liposomal doxorubicin (LIP-DOX), curcumin (LIP-CUR) and glutathione (LIP-GSH) in a dose of 5mg/kg IP daily for 1 month and were compared with their non-liposomal analogue. Concomitant supplementation with the aforementioned liposomal-loaded compounds impact on lung cancer was estimated via monitoring microRNA biomarkers including miR-122-5P and SNORD-78, pro-inflammatory biomarker Survivin, apoptotic and cell survival biomarkers including fms-related tyrosine kinase 3 (FLT-3), jasnus Janus kinase-2 (JAK-2), Phosphatidylinositol-3-kinase (PI3K), serine–threonine protein kinase (AKT) and tumor suppressor protein (P53). Liposomal-loaded doxorubicin, curcumin and glutathione significantly modulated these previously deviated genes as compared with their non-liposomal analogue, in addition to modulating lipid peroxide (LPOO) and total antioxidant capacity (TAC). MiR-122-5P and SNORD-78 were also amended reflecting the prospective impact of liposomal-loaded-nano-medicine on lung cancer treatment via up regulating P53 and down regulating PI3K/AKT/JAK2/FLT3 signaling pathway. |
| format | Article |
| id | doaj-art-4e2c627eeb904c91b6648429b1f10349 |
| institution | Kabale University |
| issn | 1868-6958 1868-6966 |
| language | English |
| publishDate | 2025-06-01 |
| publisher | BMC |
| record_format | Article |
| series | Cancer Nanotechnology |
| spelling | doaj-art-4e2c627eeb904c91b6648429b1f103492025-08-20T03:47:24ZengBMCCancer Nanotechnology1868-69581868-69662025-06-0116112610.1186/s12645-025-00331-4Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancerMai O. Kadry0Rehab M. Abdel-Megeed1Therapeutic Chemistry Department, National Research CenterTherapeutic Chemistry Department, National Research CenterAbstract Micro-RNAs (mi-RNAs) can regulate various tumor suppressor genes or oncogenes thus they were monitored in various types of cell carcinoma. Lung cancer extensive progress has led not only to understanding the molecular pathways governing human lung cancer, but it has also created a vast reservoir for alternative development of novel liposomal Nano-medicines counteracting this malignancy. Liposomal drug delivery system can passively accrue in cancer cells via the retention phenomenon and enhanced permeability. This article highlighted liposomal-loaded nano-medicine as a potential treatment for lung cancer and clarifies the correlated miRNA and mRNA gene profile. Lung cancer was induced experimentally in rats via 3-methylcholanthrene (3-MCA) in a dose of 40 mg IV for 4 months followed by treatment via certain liposomal-loaded compounds, namely, liposomal doxorubicin (LIP-DOX), curcumin (LIP-CUR) and glutathione (LIP-GSH) in a dose of 5mg/kg IP daily for 1 month and were compared with their non-liposomal analogue. Concomitant supplementation with the aforementioned liposomal-loaded compounds impact on lung cancer was estimated via monitoring microRNA biomarkers including miR-122-5P and SNORD-78, pro-inflammatory biomarker Survivin, apoptotic and cell survival biomarkers including fms-related tyrosine kinase 3 (FLT-3), jasnus Janus kinase-2 (JAK-2), Phosphatidylinositol-3-kinase (PI3K), serine–threonine protein kinase (AKT) and tumor suppressor protein (P53). Liposomal-loaded doxorubicin, curcumin and glutathione significantly modulated these previously deviated genes as compared with their non-liposomal analogue, in addition to modulating lipid peroxide (LPOO) and total antioxidant capacity (TAC). MiR-122-5P and SNORD-78 were also amended reflecting the prospective impact of liposomal-loaded-nano-medicine on lung cancer treatment via up regulating P53 and down regulating PI3K/AKT/JAK2/FLT3 signaling pathway.https://doi.org/10.1186/s12645-025-00331-4Lung cancerLiposomal nano-medicineJAK2FLT-3SurvivinSNORD78 |
| spellingShingle | Mai O. Kadry Rehab M. Abdel-Megeed Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancer Cancer Nanotechnology Lung cancer Liposomal nano-medicine JAK2 FLT-3 Survivin SNORD78 |
| title | Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancer |
| title_full | Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancer |
| title_fullStr | Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancer |
| title_full_unstemmed | Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancer |
| title_short | Novel insights into SNORD-78 and miR-122-5P the predicted diagnostic indexes of lung cancer: drug-loaded liposome formulations competing methylcholanthrene-induced lung cancer |
| title_sort | novel insights into snord 78 and mir 122 5p the predicted diagnostic indexes of lung cancer drug loaded liposome formulations competing methylcholanthrene induced lung cancer |
| topic | Lung cancer Liposomal nano-medicine JAK2 FLT-3 Survivin SNORD78 |
| url | https://doi.org/10.1186/s12645-025-00331-4 |
| work_keys_str_mv | AT maiokadry novelinsightsintosnord78andmir1225pthepredicteddiagnosticindexesoflungcancerdrugloadedliposomeformulationscompetingmethylcholanthreneinducedlungcancer AT rehabmabdelmegeed novelinsightsintosnord78andmir1225pthepredicteddiagnosticindexesoflungcancerdrugloadedliposomeformulationscompetingmethylcholanthreneinducedlungcancer |