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Title: Use of Macrophages to Target Therapeutic Adenovirus to Human Prostate Tumors
Authors: Muthana, Munitta
Giannoudis, Athina
Scott, Simon D.
Fang, Hsin-Yu
Coffelt, Seth B.
Morrow, Fiona J.
Murdoch, Craig
Burton, Julian
Cross, Neil
Burke, Bernard
Mistry, Roshna
Hamdy, Freddie
Brown, Nicola J.
Georgopoulos, Lindsay
Hoskin, Peter
Essand, Magnus
Lewis, Claire E.
Maitland, Norman J.
First Published: 13-Jan-2011
Publisher: American Association for Cancer Research
Citation: Cancer Research, 2011, 71 (5), pp. 1805-1815.
Abstract: New therapies are required to target hypoxic areas of tumors as these sites are highly resistant to conventional cancer therapies. Monocytes continuously extravasate from the bloodstream into tumors where they differentiate into macrophages and accumulate in hypoxic areas, thereby opening up the possibility of using these cells as vehicles to deliver gene therapy to these otherwise inaccessible sites. We describe a new cell-based method that selectively targets an oncolytic adenovirus to hypoxic areas of prostate tumors. In this approach, macrophages were cotransduced with a hypoxia-regulated E1A/B construct and an E1A-dependent oncolytic adenovirus, whose proliferation is restricted to prostate tumor cells using prostate-specific promoter elements from the TARP, PSA, and PMSA genes. When such cotransduced cells reach an area of extreme hypoxia, the E1A/B proteins are expressed, thereby activating replication of the adenovirus. The virus is subsequently released by the host macrophage and infects neighboring tumor cells. Following systemic injection into mice bearing subcutaneous or orthotopic prostate tumors, cotransduced macrophages migrated into hypoxic tumor areas, upregulated E1A protein, and released multiple copies of adenovirus. The virus then infected neighboring cells but only proliferated and was cytotoxic in prostate tumor cells, resulting in the marked inhibition of tumor growth and reduction of pulmonary metastases. This novel delivery system employs 3 levels of tumor specificity: the natural “homing” of macrophages to hypoxic tumor areas, hypoxia-induced proliferation of the therapeutic adenovirus in host macrophages, and targeted replication of oncolytic virus in prostate tumor cells.
DOI Link: 10.1158/0008-5472.CAN-10-2349
ISSN: 0008-5472
Type: Article
Rights: This paper was published as Cancer Research, 2011, 71 (5), pp. 1805-1815. It is available from Doi: 10.1158/0008-5472.CAN-10-2349
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation

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