File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1111/liv.12963
- Scopus: eid_2-s2.0-84963964074
- WOS: WOS:000374770600016
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Anti-CD47 antibody suppresses tumor growth and augments the effect of chemotherapy treatment in hepatocellular carcinoma
Title | Anti-CD47 antibody suppresses tumor growth and augments the effect of chemotherapy treatment in hepatocellular carcinoma |
---|---|
Authors | |
Keywords | CD47 Chemoresistance HCC |
Issue Date | 2016 |
Publisher | Wiley-Blackwell Publishing, Inc. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=1478-3223&site=1 |
Citation | Liver International, 2016, v. 36 n. 5, p. 737–745 How to Cite? |
Abstract | BACKGROUND & AIMS: Hepatocellular carcinoma (HCC) is often associated with metastasis and recurrence leading to a poor prognosis. Therefore, development of novel treatment regimens is urgently needed to improve the survival of HCC patients. In this study, we aimed to investigate the in vitro and in vivo effects of anti-CD47 antibody alone and in combination with chemotherapy in HCC. METHODS: In this study, we examined the functional effects of anti-CD47 antibody (B6H12) on cell proliferation, sphere formation, migration and invasion, chemosensitivity, macrophage-mediated phagocytosis, and tumorigenicity both in vitro and in vivo. The therapeutic efficacy of anti-CD47 antibody alone or in combination with doxorubicin was examined in patient-derived HCC xenograft. RESULTS: Blocking CD47 with anti-CD47 monoclonal antibody (B6H12) at 10mug/mL could suppress self-renewal, tumorigenicity and migration and invasion abilities of MHCC-97L and Huh-7 cells. Interestingly, anti-CD47 antibody synergized the effect of HCC cells to chemotherapeutic drugs including doxorubicin and cisplatin. Blockade of CD47 by anti-CD47 antibody induced macrophage-mediated phagocytosis. Using a patient-derived HCC xenograft mouse model, we found that anti-CD47 antibody (400mug/mouse) in combination with doxorubicin (2mg/kg) exerted maximal effects on tumor suppression, as compared with doxorubicin and anti-CD47 antibody alone. CONCLUSIONS: Anti-CD47 antibody treatment could complement chemotherapy which may be a promising therapeutic strategy for the treatment of HCC patients. This article is protected by copyright. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/220233 |
ISSN | 2023 Impact Factor: 6.0 2023 SCImago Journal Rankings: 2.087 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lo, J | - |
dc.contributor.author | Lau, YT | - |
dc.contributor.author | So, TY | - |
dc.contributor.author | Lu, P | - |
dc.contributor.author | Chan, VSF | - |
dc.contributor.author | Cheung, CH | - |
dc.contributor.author | Ching, HH | - |
dc.contributor.author | Cheng, YLB | - |
dc.contributor.author | Ma, KF | - |
dc.contributor.author | Ng, IOL | - |
dc.contributor.author | Lee, KW | - |
dc.date.accessioned | 2015-10-16T06:33:17Z | - |
dc.date.available | 2015-10-16T06:33:17Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | Liver International, 2016, v. 36 n. 5, p. 737–745 | - |
dc.identifier.issn | 1478-3223 | - |
dc.identifier.uri | http://hdl.handle.net/10722/220233 | - |
dc.description.abstract | BACKGROUND & AIMS: Hepatocellular carcinoma (HCC) is often associated with metastasis and recurrence leading to a poor prognosis. Therefore, development of novel treatment regimens is urgently needed to improve the survival of HCC patients. In this study, we aimed to investigate the in vitro and in vivo effects of anti-CD47 antibody alone and in combination with chemotherapy in HCC. METHODS: In this study, we examined the functional effects of anti-CD47 antibody (B6H12) on cell proliferation, sphere formation, migration and invasion, chemosensitivity, macrophage-mediated phagocytosis, and tumorigenicity both in vitro and in vivo. The therapeutic efficacy of anti-CD47 antibody alone or in combination with doxorubicin was examined in patient-derived HCC xenograft. RESULTS: Blocking CD47 with anti-CD47 monoclonal antibody (B6H12) at 10mug/mL could suppress self-renewal, tumorigenicity and migration and invasion abilities of MHCC-97L and Huh-7 cells. Interestingly, anti-CD47 antibody synergized the effect of HCC cells to chemotherapeutic drugs including doxorubicin and cisplatin. Blockade of CD47 by anti-CD47 antibody induced macrophage-mediated phagocytosis. Using a patient-derived HCC xenograft mouse model, we found that anti-CD47 antibody (400mug/mouse) in combination with doxorubicin (2mg/kg) exerted maximal effects on tumor suppression, as compared with doxorubicin and anti-CD47 antibody alone. CONCLUSIONS: Anti-CD47 antibody treatment could complement chemotherapy which may be a promising therapeutic strategy for the treatment of HCC patients. This article is protected by copyright. All rights reserved. | - |
dc.language | eng | - |
dc.publisher | Wiley-Blackwell Publishing, Inc. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=1478-3223&site=1 | - |
dc.relation.ispartof | Liver International | - |
dc.rights | This is the accepted version of the following article: Liver International, 2016, v. 36 n. 5, p. 737–745, which has been published in final form at http://onlinelibrary.wiley.com/wol1/doi/10.1111/liv.12963/abstract | - |
dc.subject | CD47 | - |
dc.subject | Chemoresistance | - |
dc.subject | HCC | - |
dc.title | Anti-CD47 antibody suppresses tumor growth and augments the effect of chemotherapy treatment in hepatocellular carcinoma | - |
dc.type | Article | - |
dc.identifier.email | Lo, J: jlo88@hku.hk | - |
dc.identifier.email | Lau, YT: eytlau@hku.hk | - |
dc.identifier.email | So, TY: soty@hku.hk | - |
dc.identifier.email | Chan, VSF: sfvchan@hku.hk | - |
dc.identifier.email | Ching, HH: hhching@hku.hk | - |
dc.identifier.email | Ng, IOL: iolng@hku.hk | - |
dc.identifier.email | Lee, KW: tkwlee@hkucc.hku.hk | - |
dc.identifier.authority | Chan, VSF=rp01459 | - |
dc.identifier.authority | Ng, IOL=rp00335 | - |
dc.identifier.authority | Lee, KW=rp00447 | - |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1111/liv.12963 | - |
dc.identifier.scopus | eid_2-s2.0-84963964074 | - |
dc.identifier.hkuros | 255356 | - |
dc.identifier.volume | 36 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 737 | - |
dc.identifier.epage | 745 | - |
dc.identifier.isi | WOS:000374770600016 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1478-3223 | - |