Natural products and long non-coding RNAs in prostate cancer: insights into etiology and treatment resistance

被引:4
作者
Elimam, Hanan [1 ]
Zaki, Mohamed Bakr [1 ]
Abd-Elmawla, Mai A. [2 ]
Darwish, Hebatallah A. [2 ,3 ]
Hatawsh, Abdulrahman [4 ]
Aborehab, Nora M. [5 ]
Mageed, Sherif S. Abdel [6 ]
Moussa, Rewan [7 ]
Mohammed, Osama A. [8 ]
Abdel-Reheim, Mustafa Ahmed [9 ]
Doghish, Ahmed S. [10 ,11 ]
机构
[1] Univ Sadat City, Fac Pharm, Dept Biochem, Sadat City 32897, Egypt
[2] Cairo Univ, Fac Pharm, Dept Biochem, Cairo, Egypt
[3] Future Univ Egypt, Fac Pharm, Pharmacol Toxicol & Biochem Dept, Cairo, Egypt
[4] Nile Univ, Biotechnol Sch, 26th July Corridor, Sheikh Zayed City 12588, Giza, Egypt
[5] Ahram Canadian Univ, Fac Pharm, Biochem Dept, Giza, Egypt
[6] Badr Univ Cairo BUC, Fac Pharm, Pharmacol & Toxicol Dept, Badr City 11829, Cairo, Egypt
[7] Helwan Univ, Sch Fac Med, Cairo 11795, Egypt
[8] Univ Bisha, Coll Med, Dept Pharmacol, Bisha 61922, Saudi Arabia
[9] Shaqra Univ, Coll Pharm, Dept Pharmacol, Shaqra 11961, Saudi Arabia
[10] Badr Univ Cairo BUC, Fac Pharm, Dept Biochem, Badr City 11829, Cairo, Egypt
[11] Al Azhar Univ, Fac Pharm Boys, Biochem & Mol Biol Dept, Nasr City 11231, Cairo, Egypt
关键词
Prostate cancer; LncRNA; Chemotherapy; Diagnosis; Natural product; CELL-PROLIFERATION; POOR-PROGNOSIS; ANDROGEN RECEPTOR; HOMOLOGOUS RECOMBINATION; REGULATES PROLIFERATION; MESENCHYMAL TRANSITION; THERAPEUTIC TARGET; COLORECTAL-CANCER; SIGNALING PATHWAY; UP-REGULATION;
D O I
10.1007/s00210-024-03736-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Globally, the incidence and death rates associated with cancer persist in rising, despite considerable advancements in cancer therapy. Although some malignancies are manageable by a mix of chemotherapy, surgery, radiation, and targeted therapy, most malignant tumors either exhibit poor responsiveness to early identification or endure post-treatment survival. The prognosis for prostate cancer (PCa) is unfavorable since it is a perilous and lethal malignancy. The capacity of phytochemical and nutraceutical chemicals to repress oncogenic lncRNAs and activate tumor suppressor lncRNAs has garnered significant attention as a possible strategy to diminish the development, proliferation, metastasis, and invasion of cancer cells. A potential technique to treat cancer and enhance the sensitivity of cancer cells to existing conventional therapies is the use of phytochemicals with anticancer characteristics. Functional studies indicate that lncRNAs modulate drug resistance, stemness, invasion, metastasis, angiogenesis, and proliferation via interactions with tumor suppressors and oncoproteins. Among them, numerous lncRNAs, such as HOTAIR, PlncRNA1, GAS5, MEG3, LincRNA-21, and POTEF-AS1, support the development of PCa through many molecular mechanisms, including modulation of tumor suppressors and regulation of various signal pathways like PI3K/Akt, Bax/Caspase 3, P53, MAPK cascade, and TGF-beta 1. Other lncRNAs, in particular, MALAT-1, CCAT2, DANCR, LncRNA-ATB, PlncRNA1, LincRNA-21, POTEF-AS1, ZEB1-AS1, SChLAP1, and H19, are key players in regulating the aforementioned processes. Natural substances have shown promising anticancer benefits against PCa by altering essential signaling pathways. The overexpression of some lncRNAs is associated with advanced TNM stage, metastasis, chemoresistance, and reduced survival. LncRNAs possess crucial clinical and transitional implications in PCa, as diagnostic and prognostic biomarkers, as well as medicinal targets. To impede the progression of PCa, it is beneficial to target aberrant long non-coding RNAs using antisense oligonucleotides or small interfering RNAs (siRNAs). This prevents them from transmitting harmful messages. In summary, several precision medicine approaches may be used to rectify dysfunctional lncRNA regulatory circuits, so improving early PCa detection and eventually facilitating the conquest of this lethal disease. Due to their presence in biological fluids and tissues, they may serve as novel biomarkers. Enhancing PCa treatments mitigates resistance to chemotherapy and radiation.
引用
收藏
页码:6349 / 6368
页数:20
相关论文
共 167 条
[1]   Association of XIST/miRNA155/Gab2/TAK1 cascade with the pathogenesis of anti-phospholipid syndrome and its effect on cell adhesion molecules and inflammatory mediators [J].
Abd-Elmawla, Mai A. ;
Elsabagh, Yumn A. ;
Aborehab, Nora M. .
SCIENTIFIC REPORTS, 2023, 13 (01)
[2]   Acovenoside A as a novel therapeutic approach to boost taxol and carboplatin apoptotic and antiproliferative activities in NSCLC: Interplay of miR-630/miR-181a and apoptosis genes [J].
Aborehab, Nora M. ;
Abd-Elmawla, Mai A. ;
ElSayed, Abeer M. ;
Sabry, Omar ;
Ezzat, Shahira M. .
BIOORGANIC CHEMISTRY, 2023, 139
[3]   Targeting the MALAT1 gene with the CRISPR/Cas9 technique in prostate cancer [J].
Ahmadi-Balootaki, Soraya ;
Doosti, Abbas ;
Jafarinia, Mojtaba ;
Goodarzi, Hamed Reza .
GENES AND ENVIRONMENT, 2022, 44 (01)
[4]   Autophagy: A challengeable paradox in cancer treatment [J].
Ahmadi-Dehlaghi, Farnaz ;
Mohammadi, Parisa ;
Valipour, Elahe ;
Pournaghi, Pouya ;
Kiani, Sarah ;
Mansouri, Kamran .
CANCER MEDICINE, 2023, 12 (10) :11542-11569
[5]   Long Noncoding RNAs CAT2064 and CAT2042 may Function as Diagnostic Biomarkers for Prostate Cancer by Affecting Target MicrorRNAs [J].
Amirmahani, Farzane ;
Ebrahimi, Nasim ;
Askandar, Rafee Habib ;
Eshkaftaki, Marzieh Rasouli ;
Fazeli, Katayoun ;
Hamblin, Michael R. .
INDIAN JOURNAL OF CLINICAL BIOCHEMISTRY, 2024, 39 (03) :322-330
[6]   Evolving standards in the treatment of docetaxel-refractory castration-resistant prostate cancer [J].
Antonarakis, E. S. ;
Armstrong, A. J. .
PROSTATE CANCER AND PROSTATIC DISEASES, 2011, 14 (03) :192-205
[7]   Molecular panorama of therapy resistance in prostate cancer: a pre-clinical and bioinformatics analysis for clinical translation [J].
Ashrafizadeh, Milad ;
Zhang, Wei ;
Tian, Yu ;
Sethi, Gautam ;
Zhang, Xianbin ;
Qiu, Aiming .
CANCER AND METASTASIS REVIEWS, 2024, 43 (01) :229-260
[8]   Contemporary Role of Prostate Cancer Antigen 3 in the Management of Prostate Cancer [J].
Auprich, Marco ;
Bjartell, Anders ;
Chun, Felix K. -H. ;
de la Taille, Alexandre ;
Freedland, Stephen J. ;
Haese, Alexander ;
Schalken, Jack ;
Stenzl, Arnulf ;
Tombal, Bertrand ;
van der Poel, Henk .
EUROPEAN UROLOGY, 2011, 60 (05) :1045-1054
[9]   Molecular Basis of Prostate Cancer and Natural Products as Potential Chemotherapeutic and Chemopreventive Agents [J].
Bai, Bingke ;
Chen, Qianbo ;
Jing, Rui ;
He, Xuhui ;
Wang, Hongrui ;
Ban, Yanfei ;
Ye, Qi ;
Xu, Weiheng ;
Zheng, Chengjian .
FRONTIERS IN PHARMACOLOGY, 2021, 12
[10]   New Adenosine Derivatives from Aizoon canariense L.: In Vitro Anticholinesterase, Antimicrobial, and Cytotoxic Evaluation of Its Extracts [J].
Bakr, Riham O. ;
El-Behairy, Mohammed F. ;
Elissawy, Ahmed M. ;
Elimam, Hanan ;
Fayed, Marwa A. A. .
MOLECULES, 2021, 26 (05)