Transcriptional control of the MUC16 promoter facilitates follicle-stimulating hormone peptide-conjugated shRNA nanoparticle-mediated inhibition of ovarian carcinoma in vivo-Reference-Cited by-同舟云学术

Transcriptional control of the MUC16 promoter facilitates follicle-stimulating hormone peptide-conjugated shRNA nanoparticle-mediated inhibition of ovarian carcinoma in vivo

Published:2018-01-01 Issue:1 Volume:25 Page:797-806
ISSN:1071-7544
Container-title:Drug Delivery
language:en
Short-container-title:Drug Delivery

Author:

Zhang Ming-Xing¹,Hong Shan-Shan¹,Cai Qing-Qing¹²³,Zhang Meng¹,Chen Jun⁴,Zhang Xiao-Yan¹²³^ORCID,Xu Cong-Jian¹²³^ORCID

Affiliation:

1. Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China;

2. Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, Shanghai, China;

3. Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Shanghai, China;

4. Department of Pharmaceutics, School of Pharmacy, Fudan University, Shanghai, China

Funder

National Natural Sciences Foundation of China

National Key R&D Program of China

Youth Talent Foundation of Shanghai Health System

Shanghai Medical Center of Key Programs for Female Reproductive Diseases

Publisher

Informa UK Limited

Subject

Pharmaceutical Science,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/10717544.2018.1451934

Reference36 articles.

1. More than a biomarker: CA125 may contribute to ovarian cancer pathogenesis

2. Conflicting Views on the Molecular Structure of the Cancer Antigen CA125/MUC16

3. Understanding the Unique Attributes of MUC16 (CA125): Potential Implications in Targeted Therapy

4. Dual E1A oncolytic adenovirus: targeting tumor heterogeneity with two independent cancer-specific promoter elements, DF3/MUC1 and hTERT

5. In vivo Radioiodide Imaging and Treatment of Breast Cancer Xenografts after MUC1-Driven Expression of the Sodium Iodide Symporter

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