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
[91]   Transforming growth factor-beta (TGF-β) in prostate cancer: A dual function mediator? [J].
Mirzaei, Sepideh ;
Paskeh, Mahshid Deldar Abad ;
Saghari, Yalda ;
Zarrabi, Ali ;
Hamblin, Michael R. ;
Entezari, Maliheh ;
Hashemi, Mehrdad ;
Aref, Amir Reza ;
Hushmandi, Kiavash ;
Kumar, Alan Prem ;
Rabiee, Navid ;
Ashrafizadeh, Milad ;
Samarghandian, Saeed .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2022, 206 :435-452
[92]   Long non-coding RNAs and prostate cancer [J].
Misawa, Aya ;
Takayama, Ken-ichi ;
Inoue, Satoshi .
CANCER SCIENCE, 2017, 108 (11) :2107-2114
[93]   Androgen-induced lncRNA POTEF-AS1 regulates apoptosis-related pathway to facilitate cell survival in prostate cancer cells [J].
Misawa, Aya ;
Takayama, Ken-ichi ;
Fujimura, Tetsuya ;
Homma, Yukio ;
Suzuki, Yutaka ;
Inoue, Satoshi .
CANCER SCIENCE, 2017, 108 (03) :373-379
[94]   Androgen-induced Long Noncoding RNA (lncRNA) SOCS2-AS1 Promotes Cell Growth and Inhibits Apoptosis in Prostate Cancer Cells [J].
Misawa, Aya ;
Takayama, Ken-ichi ;
Urano, Tomohiko ;
Inoue, Satoshi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (34) :17861-17880
[95]  
Na XY, 2015, INT J CLIN EXP MED, V8, P12609
[96]   Mechanisms of Therapeutic Resistance in Prostate Cancer [J].
Nakazawa, Mary ;
Paller, Channing ;
Kyprianou, Natasha .
CURRENT ONCOLOGY REPORTS, 2017, 19 (02)
[97]   Long Noncoding RNA NEAT1 as a Potential Candidate Biomarker for Prostate Cancer [J].
Nitusca, Diana ;
Marcu, Anca ;
Dema, Alis ;
Balacescu, Loredana ;
Balacescu, Ovidiu ;
Bardan, Razvan ;
Cumpanas, Alin Adrian ;
Sirbu, Ioan Ovidiu ;
Petrut, Bogdan ;
Seclaman, Edward ;
Marian, Catalin .
LIFE-BASEL, 2021, 11 (04)
[98]   Crosstalk of the Androgen Receptor with Transcriptional Collaborators: Potential Therapeutic Targets for Castration-Resistant Prostate Cancer [J].
Obinata, Daisuke ;
Takayama, Kenichi ;
Takahashi, Satoru ;
Inoue, Satoshi .
CANCERS, 2017, 9 (03)
[99]   Epithelial-Mesenchymal Transition (EMT) and Prostate Cancer [J].
Odero-Marah, Valerie ;
Hawsawi, Ohuod ;
Henderson, Veronica ;
Sweeney, Janae .
CELL & MOLECULAR BIOLOGY OF PROSTATE CANCER: UPDATES, INSIGHTS AND NEW FRONTIERS, 2018, 1095 :101-110
[100]   Antisense transcription at the TRPM2 locus as a novel prognostic marker and therapeutic target in prostate cancer [J].
Orfanelli, U. ;
Jachetti, E. ;
Chiacchiera, F. ;
Grioni, M. ;
Brambilla, P. ;
Briganti, A. ;
Freschi, M. ;
Martinelli-Boneschi, F. ;
Doglioni, C. ;
Montorsi, F. ;
Bellone, M. ;
Casari, G. ;
Pasini, D. ;
Lavorgna, G. .
ONCOGENE, 2015, 34 (16) :2094-2102