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Exosomes derived from HIV-1-infected cells promote growth and progression of cancer via HIV TAR RNA.


ABSTRACT: People living with HIV/AIDS on antiretroviral therapy have increased risk of non-AIDS-defining cancers (NADCs). However, the underlying mechanism for development and progression of certain NADCs remains obscure. Here we show that exosomes released from HIV-infected T cells and those purified from blood of HIV-positive patients stimulate proliferation, migration and invasion of oral/oropharyngeal and lung cancer cells. The HIV transactivation response (TAR) element RNA in HIV-infected T-cell exosomes is responsible for promoting cancer cell proliferation and inducing expression of proto-oncogenes and Toll-like receptor 3 (TLR3)-inducible genes. These effects depend on the loop/bulge region of the molecule. HIV-infected T-cell exosomes rapidly enter recipient cells through epidermal growth factor receptor (EGFR) and stimulate ERK1/2 phosphorylation via the EGFR/TLR3 axis. Thus, our findings indicate that TAR RNA-containing exosomes from HIV-infected T cells promote growth and progression of particular NADCs through activation of the ERK cascade in an EGFR/TLR3-dependent manner.

SUBMITTER: Chen L 

PROVIDER: S-EPMC6214989 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Exosomes derived from HIV-1-infected cells promote growth and progression of cancer via HIV TAR RNA.

Chen Lechuang L   Feng Zhimin Z   Yue Hong H   Bazdar Douglas D   Mbonye Uri U   Zender Chad C   Harding Clifford V CV   Bruggeman Leslie L   Karn Jonathan J   Sieg Scott F SF   Wang Bingcheng B   Jin Ge G  

Nature communications 20181102 1


People living with HIV/AIDS on antiretroviral therapy have increased risk of non-AIDS-defining cancers (NADCs). However, the underlying mechanism for development and progression of certain NADCs remains obscure. Here we show that exosomes released from HIV-infected T cells and those purified from blood of HIV-positive patients stimulate proliferation, migration and invasion of oral/oropharyngeal and lung cancer cells. The HIV transactivation response (TAR) element RNA in HIV-infected T-cell exos  ...[more]

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