Tumor acidic microenvironment activatable DNA nanostructure for precise cancer cell targeting and inhibition
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作者:
Yanfei Liu
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Department of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South UniversityDepartment of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South University
Yanfei Liu
[1
]
Yaqin Hu
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Department of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South UniversityDepartment of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South University
Yaqin Hu
[1
]
Yifu Tan
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机构:
Xiangya School of Pharmaceutical Sciences, Central South UniversityDepartment of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South University
Yifu Tan
[2
]
Qiwen Chen
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Department of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South UniversityDepartment of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South University
Qiwen Chen
[1
]
Zhenbao Liu
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Xiangya School of Pharmaceutical Sciences, Central South University
Molecular Imaging Research Center of Central SouthDepartment of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South University
Zhenbao Liu
[2
,3
]
机构:
[1] Department of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South University
[2] Xiangya School of Pharmaceutical Sciences, Central South University
[3] Molecular Imaging Research Center of Central South
Precise tumor targeting and therapy is a major trend in cancer treatment. Herein, we designed a tumor acidic microenvironment activatable drug loaded DNA nanostructure, in which, we made a clever use of the sequences of AS1411 and i-motif, which can partially hybridize, and designed a simple while robust DNA D-strand nanostructure, in which, i-motif sequence was designed to regulate the binding ability of the AS1411 aptamer to target tumor. In the normal physiological environment, i-motif inhibits the targeting ability of AS1411. In the acidic tumor microenvironment, i-motif forms a quadruplex conformation and dissociates from AS1411, restoring the targeting ability of AS1411. Only when acidic condition and tumor cell receptor are present, this nanostructure can be internalized by the tumor cells. Moreover, the structure change of this nanostructure can realize the release of loaded drug. This drug loaded A-I-Duplex DNA structure showed cancer cell and spheroid targeting and inhibition ability, which is promising in the clinical cancer therapy.
机构:
Cent South Univ, Coll Chem & Chem Engn, Dept Pharmaceut Engn, Changsha 410083, Peoples R ChinaCent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R China
Liu, Yanfei
Hu, Yaqin
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Cent South Univ, Coll Chem & Chem Engn, Dept Pharmaceut Engn, Changsha 410083, Peoples R ChinaCent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R China
Hu, Yaqin
Tan, Yifu
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机构:
Cent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R ChinaCent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R China
Tan, Yifu
Chen, Qiwen
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机构:
Cent South Univ, Coll Chem & Chem Engn, Dept Pharmaceut Engn, Changsha 410083, Peoples R ChinaCent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R China
Chen, Qiwen
Liu, Zhenbao
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机构:
Cent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R China
Cent South Univ, Mol Imaging Res Ctr, Changsha 410008, Peoples R ChinaCent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R China
机构:
Middle East Univ, Fac Pharm, Amman 11831, JordanMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Saadh, Mohamed J.
Mustafa, Mohammed Ahmed
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机构:
Univ Imam Jaafar AL Sadiq, Dept Med Lab Technol, Tehran, IraqMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Mustafa, Mohammed Ahmed
Qassem, Laith Yassen
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机构:
Al Noor Univ Coll, Dept Med Lab Tech, Nineveh, IraqMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Qassem, Laith Yassen
Ghadir, Ghadir Kamil
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机构:
Al Farahidi Univ, Coll Pharm, Baghdad, IraqMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Ghadir, Ghadir Kamil
Alaraj, Mohd
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机构:
Jerash Private Univ, Fac Pharm, Jerash, JordanMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Alaraj, Mohd
Alubiady, Mahmood Hasen Shuhata
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机构:
Al Hadi Univ Coll, Dept Med Engn, Baghdad 10011, IraqMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Alubiady, Mahmood Hasen Shuhata
Al-Abdeen, Salah Hassan Zain
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机构:
AL Nisour Univ Coll, Dept Med Labs Technol, Baghdad, IraqMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Al-Abdeen, Salah Hassan Zain
Shakier, Hussein Ghafel
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机构:
Natl Univ Sci & Technol, Coll Pharm, Dhi Qar, IraqMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Shakier, Hussein Ghafel
Alshahrani, Mohammad Y.
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机构:
King Khalid Univ, Coll Appl Med Sci, Dept Clin Lab Sci, Abha, Saudi ArabiaMiddle East Univ, Fac Pharm, Amman 11831, Jordan
Alshahrani, Mohammad Y.
Zwamel, Ahmed Hussein
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机构:
Islamic Univ, Med Lab Tech Coll, Najaf, Iraq
Islamic Univ Al Diwaniyah, Med Lab Tech Coll, Al Diwaniyah, Iraq
Islamic Univ Babylon, Med Lab Tech Coll, Babylon, IraqMiddle East Univ, Fac Pharm, Amman 11831, Jordan
机构:
NCI, Stem Cell Regulat & Anim Aging Sect, Basic Res Lab, Frederick, MD 21702 USANCI, Stem Cell Regulat & Anim Aging Sect, Basic Res Lab, Frederick, MD 21702 USA
Singh, Shree Ram
Rameshwar, Pranela
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机构:
Rutgers, New Jersey Med Sch, Dept Med Hematol Oncol, Newark, NJ 07103 USANCI, Stem Cell Regulat & Anim Aging Sect, Basic Res Lab, Frederick, MD 21702 USA
Rameshwar, Pranela
Siegel, Peter
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机构:
McGill Univ, Dept Med Biochem & Anat & Cell Biol, Rosalind & Morris Goodman Canc Res Ctr, Montreal, PQ H3A 1A3, CanadaNCI, Stem Cell Regulat & Anim Aging Sect, Basic Res Lab, Frederick, MD 21702 USA