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We found that shRNA down-regulation of Metnase levels markedly sensitized these breast cancer cells to adriamycin-induced apoptosis (Fig. 3C).
Indeed, SNS-032 markedly sensitized HeLa and A549 cells to TRAIL-induced cell death.
Bcl2l1 knockdown did not increase basal α cell apoptosis (Fig. 5D), but it markedly sensitized the cells to palmitate.
Blockade of caspase-8 with zVAD-fmk or IETD-fmk markedly sensitized microglia to TNF and TLR1/2, TLR3, TLR4, and TLR7/8 ligation.
In contrast, caspase blockade did not prevent LPS-induced TNF secretion in primary rat microglia, but rather markedly sensitized the cells to LPS challenge.
In two other estrogen-deprived breast cancer lines, LTED and E8CASS, basal Bcl-2 level was greatly elevated and knockdown of Bcl-2 expression with siRNA markedly sensitized these cells to the apoptotic action of E2 [ 32].
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Here, we show that MK-8776 markedly sensitizes multiple cell lines to gemcitabine.
Moreover, silencing of RRM2 by siRNA could enhance the DNA damage and markedly sensitize HCT-116 cells to camptothecin, a topoisomerase I inhibitor [ 47].
For example, PANDA interacts with the transcription factor NF-YA to limit the expression of pro-apoptotic genes; PANDA depletion markedly sensitizes human fibroblasts to apoptosis by doxorubicin.
Oxidative stress markedly sensitizes mitochondria toward mitochondrial membrane permeabilization induction and can also cause damage to nucleic acids and proteins [ 14].
Although TNF-α is not currently an anticancer agent for treatment of human cancers (because of side effects such as normal cell toxicity), low doses of TNF-α can markedly sensitize cancer cells to chemotherapy-induced apoptosis [ 26, 27].
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