Cited by 109Seaweed-derived Bioactive CompoundsT-cell and Retrovirus StudiesPolysaccharides Composition and Applications

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Anti-viral activity of red microalgal polysaccharides against retroviruses

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Talyshinsky, Marina M, Souprun, Yelena Y, Huleihel, Mahmoud M·2002·Cancer Cell International

DOI 10.1186/1475-2867-2-8PMC PMC140136

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Abstract

Red microalgal polysaccharides significantly inhibited the production of retroviruses (murine leukemia virus- MuLV) and cell transformation by murine sarcoma virus(MuSV-124) in cell culture. The most effective inhibitory effect of these polysaccharides against both cell transformation and virus production was obtained when the polysaccharide was added 2 h before or at the time of infection. Although, addition of the polysaccharide post-infection significantly reduced the number of transformed cells, but its effect was less marked than that obtained when the polysaccharide was added before or at the time of infection.The finding that the inhibition of cell transformation by MuSV-124 was reversible after removal of the polysaccharide suggested that microalgal polysaccharides inhibited a late step after provirus integration into the host genome. In conclusion, our findings could support the possibility that the polysaccharide may affect early steps in the virus replication cycle, such as virus absorption into the host cells, in addition to its effect on a late step after provirus integration.

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TEMIN, H. M., & MIZUTANI, S. (1970) · Nature · doi:10.1038/2261211a0 · Cited by 2,128
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BALTIMORE, D. (1970) · Nature · doi:10.1038/2261209a0 · Cited by 2,068
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Witvrouw, M., & Clercq, E. D. (1997) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(96)00563-0 · Cited by 531
Plant Physiology and Biochemistry
Metcalfe, C. R., & Whittingham, C. P. (1965) · Kew Bulletin · doi:10.2307/4108213 · Cited by 522
Current lead natural products for the chemotherapy of human immunodeficiency virus (HIV) infection
Clercq, E. D. (2000) · Medicinal Research Reviews · doi:10.1002/1098-1128(200009)20:5 · Cited by 358
Anti-HIV Activity of Extracts and Compounds from Algae and Cyanobacteria
Schaeffer, D. J., & Krylov, V. S. (2000) · Ecotoxicology and Environmental Safety · doi:10.1006/eesa.1999.1862 · Cited by 326
Comprehensive Virology
Epstein, M. A. (1976) · British Journal of Cancer · doi:10.1038/bjc.1976.198 · Cited by 291
Stimulation of humoral and cell mediated immunity by polysaccharide from mushroom phellinus linteus
Kim, H. M., Han, S., Oh, G. T., Kim, Y. H., Hong, D. H., Hong, N. D., & Yoo, I. D. (1996) · International Journal of Immunopharmacology · doi:10.1016/0192-0561(96)00028-8 · Cited by 235
Marine algae in pharmaceutical science
Hoppe, H. A., Levring, T., & Tanaka, Y. (1979) · De Gruyter eBooks · Cited by 225
Identification and characterization of HIV-specific RNase H by monoclonal antibody
Hansen, J., Schulze, T., Mellert, W., & Moelling, K. (1988) · The EMBO Journal · doi:10.1002/j.1460-2075.1988.tb02805.x · Cited by 190

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Authors: Talyshinsky, M. M., Souprun, Y. Y., & Huleihel, M. M.
Affiliations: Ben-Gurion University of the Negev (IL)
Corresponding author: Huleihel, Mahmoud M
ORCID: Huleihel, Mahmoud M
Venue: Cancer Cell International
Publisher: Springer Science and Business Media LLC
Published: 2002-07-05
Volume: 2
Issue: 1
Pages: 8-8
ISSN: 1475-2867 (ISSN-L)
DOI: 10.1186/1475-2867-2-8
PMC: PMC140136
OpenAlex: W2111203587
Cited by: 109
References: 39
Citations by year: 2026: 4 · 2025: 5 · 2024: 6 · 2023: 3 · 2022: 11 · 2021: 17 · 2020: 8 · 2019: 7 · 2018: 7 · 2017: 3 · 2016: 6 · 2015: 5 · 2014: 4 · 2013: 7 · 2012: 3
FWCI: 1.29
Type: journal article
Language: en
Open access: gold
doi.org
Locations: Cancer Cell International (publishedVersion)
PubMed Central (publishedVersion, other-oa)
PubMed (publishedVersion)
DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Seaweed-derived Bioactive Compounds
Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
Life Sciences › Agricultural and Biological Sciences › Food Science › Polysaccharides Composition and Applications
Keywords: retroviruses, murine leukemia virus, murine sarcoma virus, antiviral activity, viral life cycle, provirus integration

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Anti-viral activity of red microalgal polysaccharides against retroviruses

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