ASS1 regulates immune microenvironment via CXCL8 signaling in ovarian cancer
Biochemical and Biophysical Research Communications, ISSN: 0006-291X, Vol: 631, Page: 86-92
2022
- 6Citations
- 4Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations6
- Citation Indexes6
- CrossRef1
- Captures4
- Readers4
Article Description
Ovarian cancer is one of the most serious and deadly cancers for female and currently no effective screening approaches have been achieved. Therefore it is usually diagnosed at an advanced stage and most patients have a poor prognosis. The development of ovarian cancer is a comprehensive process depending on the cross-talk between the various cells in the tumor microenvironment and the immune system. Thus, the immunotherapy may be revolutionized as an effective treatment of this disease. In this study, we firstly identified ASS1 as an immunomodulatory molecule. By RNA sequencing, antibody array and animal assys, we further provided new insights into understanding the crosstalk between ovarian cancer cells and their microenvironmental immune molecules, which may suggest a new potential therapeutic target for ovarian cancer.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0006291X22011676; http://dx.doi.org/10.1016/j.bbrc.2022.08.045; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85138792218&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/36182868; https://linkinghub.elsevier.com/retrieve/pii/S0006291X22011676; https://dx.doi.org/10.1016/j.bbrc.2022.08.045
Elsevier BV
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