Palladium Nanoplate-Based IL-6 Receptor Antagonists Ameliorate Cancer-Related Anemia and Simultaneously Inhibit Cancer Progression-Reference-Cited by-同舟云学术

Palladium Nanoplate-Based IL-6 Receptor Antagonists Ameliorate Cancer-Related Anemia and Simultaneously Inhibit Cancer Progression

Published:2022-01-14 Issue:2 Volume:22 Page:751-760
ISSN:1530-6984
Container-title:Nano Letters
language:en
Short-container-title:Nano Lett.

Author:

Zhu Jianqiang¹²,Fu Qingfeng²,Wang Shunhao¹³,Ren Liting¹,Feng Wenya¹³,Wei Shuting¹³,Zhang Zhihong²,Xu Yong²,Ganz Tomas⁴,Liu Sijin¹³^ORCID

Affiliation:

1. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China

2. Department of Urology, Tianjin Institute of Urology, The Second Hospital of Tianjin Medical University, Tianjin 300211, China

3. University of Chinese Academy of Sciences, Beijing 100049, China

4. Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, California 90095, United States

Funder

Young Elite Scientists Sponsorship Program by Tianjin

National Natural Science Foundation of China

Tianjin Education Commission for Higher Education

Tianjin Research Program of Application Foundation and Advanced Technology

Publisher

American Chemical Society (ACS)

Subject

Mechanical Engineering,Condensed Matter Physics,General Materials Science,General Chemistry,Bioengineering

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.nanolett.1c04260

Reference46 articles.

2. Anaemia in cancer patients: pathophysiology, incidence and treatment

3. The European Cancer Anaemia Survey (ECAS): A large, multinational, prospective survey defining the prevalence, incidence, and treatment of anaemia in cancer patients

4. The role of inflammation, iron, and nutritional status in cancer-related anemia: results of a large, prospective, observational study

5. Recent update in the pathogenesis and treatment of chemotherapy and cancer induced anemia

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