Shanker Anil, Sayers Thomas
Cancer and Inflammation Program, SAIC-Frederick Inc., NCI-Frederick, Frederick, MD, USA.
Adv Exp Med Biol. 2007;601:163-71. doi: 10.1007/978-0-387-72005-0_17.
The molecular basis underlying tumor destruction in vivo by specific antitumor CD8+ T cells remains unclear. We propose that the local production of certain tumor necrosis factor (TNF)-family members (death ligands) may be more important for tumor destruction in vivo than previously thought. Also, the apoptotic response of some tumor cells to the TNF-family member TRAIL can be augmented by the proteasome inhibitor bortezomib (Velcade). Thus, bortezomib may sensitize tumor cells to T cell-mediated cytotoxicity and could potentially improve the beneficial effects of immunotherapy.