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Albumin Nano-Encapsulation of Piceatannol Enhances Its Anticancer Potential in Colon Cancer Via Downregulation of Nuclear p65 and HIF-1α.
Aljabali, Alaa A A; Bakshi, Hamid A; Hakkim, Faruk L; Haggag, Yusuf A; Al-Batanyeh, Khalid M; Al Zoubi, Mazhar S; Al-Trad, Bahaa; Nasef, Mohamed M; Satija, Saurabh; Mehta, Meenu; Pabreja, Kavita; Mishra, Vijay; Khan, Mohammed; Abobaker, Salem; Azzouz, Ibrahim M; Dureja, Harish; Pabari, Ritesh M; Dardouri, Ashref Ali K; Kesharwani, Prashant; Gupta, Gaurav; Dhar Shukla, Shakti; Prasher, Parteek; Charbe, Nitin B; Negi, Poonam; Kapoor, Deepak N; Chellappan, Dinesh Kumar; Webba da Silva, Mateus; Thompson, Paul; Dua, Kamal; McCarron, Paul; Tambuwala, Murtaza M.
Afiliação
  • Aljabali AAA; Department of Pharmaceutical Sciences, Yarmouk University-Faculty of Pharmacy, Irbid 566, Jordan.
  • Bakshi HA; School of Pharmacy and Pharmaceutical Science, Ulster University, Coleraine, County Londonderry, Northern Ireland BT52 1SA, UK.
  • Hakkim FL; Department of Mathematics and Sciences, College of Arts and Applied Sciences Dhofar University Salalah, Salalah 211, Oman.
  • Haggag YA; Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Tanta, Tanta 31111, Egypt.
  • Al-Batanyeh KM; Department of Biological Sciences,Yarmouk University-Faculty of Science, Irbid 566, Jordan.
  • Al Zoubi MS; Department of Basic Medical Sciences, Yarmouk University-Faculty of Medicine, Irbid 566, Jordan.
  • Al-Trad B; Department of Basic Medical Sciences, Yarmouk University-Faculty of Medicine, Irbid 566, Jordan.
  • Nasef MM; Department of Pharmacy and Biomedical Sciences, School of Applied Sciences, University of Huddersfield, Queensgate, Huddersfield HD13DH, UK.
  • Satija S; School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab 144411, India.
  • Mehta M; School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab 144411, India.
  • Pabreja K; School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab 144411, India.
  • Mishra V; School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab 144411, India.
  • Khan M; School of Pharmacy and Pharmaceutical Science, Ulster University, Coleraine, County Londonderry, Northern Ireland BT52 1SA, UK.
  • Abobaker S; Department of Gynecology, European Competence Center for Ovarian Cancer, Campus Virchow, Klinikum Charite-Universitatmedizin Berlin, augustenburger Platz 1, Berlin 13353, Germany.
  • Azzouz IM; Department of Dermatology, Venerology, and allergology, Charite-Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Chariteplatz1, Berlin 10117, Germany.
  • Dureja H; Department of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak 124001, India.
  • Pabari RM; School of Pharmacy, Royal College of Surgeons in Ireland, Dublin-09 D02 YN77, Ireland.
  • Dardouri AAK; Department of Forensic Science, School of Applied Science, Huddersfield University, Queensgate, Huddersfield HD1 3DH, UK.
  • Kesharwani P; Department of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi 110062, India.
  • Gupta G; School of Pharmacy, Suresh Gyan Vihar University, Jagatpura, Jaipur 302017, India.
  • Dhar Shukla S; Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute (HMRI) and School of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, New South Wales NSW 230, Australia.
  • Prasher P; Department of Chemistry, University of Petroleum & Energy Studies, Dehradun 248007, India.
  • Charbe NB; Departamento de Química Orgánica, Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Av. Vicuña McKenna 4860, 7820436, Macul, Santiago 4860, Chile.
  • Negi P; School of Pharmaceutical Sciences, Shoolini University of Biotechnology and Management Sciences, Solan, India 173229, India.
  • Kapoor DN; School of Pharmaceutical Sciences, Shoolini University of Biotechnology and Management Sciences, Solan, India 173229, India.
  • Chellappan DK; Department of Life Sciences, School of Pharmacy, International Medical University, Bukit Jalil, Kuala Lumpur 57000, Malaysia.
  • Webba da Silva M; School of Pharmacy and Pharmaceutical Science, Ulster University, Coleraine, County Londonderry, Northern Ireland BT52 1SA, UK.
  • Thompson P; School of Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, BT52 1SA, UK.
  • Dua K; Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute (HMRI) and School of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, New South Wales NSW 230, Australia.
  • McCarron P; School of Pharmaceutical Sciences, Shoolini University of Biotechnology and Management Sciences, Solan, India 173229, India.
  • Tambuwala MM; Discipline of Pharmacy, Graduate School of Health, University of Technology, Sydney, NSW 2007, Australia.
Cancers (Basel) ; 12(1)2020 01 01.
Article em En | MEDLINE | ID: mdl-31906321
ABSTRACT
Piceatannol (PIC) is known to have anticancer activity, which has been attributed to its ability to block the proliferation of cancer cells via suppression of the NF-kB signaling pathway. However, its effect on hypoxia-inducible factor (HIF) is not well known in cancer. In this study, PIC was loaded into bovine serum albumin (BSA) by desolvation method as PIC-BSA nanoparticles (NPs). These PIC-BSA nanoparticles were assessed for in vitro cytotoxicity, migration, invasion, and colony formation studies and levels of p65 and HIF-1α. Our results indicate that PIC-BSA NPs were more effective in downregulating the expression of nuclear p65 and HIF-1α in colon cancer cells as compared to free PIC. We also observed a significant reduction in inflammation induced by chemical colitis in mice by PIC-BSA NPs. Furthermore, a significant reduction in tumor size and number of colon tumors was also observed in the murine model of colitis-associated colorectal cancer, when treated with PIC-BSA NPs as compared to free PIC. The overall results indicate that PIC, when formulated as PIC-BSA NPs, enhances its therpautice potential. Our work could prompt further research in using natural anticancer agents as nanoparticels with possiable human clinical trails. This could lead to the development of a new line of safe and effective therapeutics for cancer patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cancers (Basel) Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cancers (Basel) Ano de publicação: 2020 Tipo de documento: Article