To probe the regulatory roles of cysteine (Cys) in cancer cell survival, a highly selective and sensitive fluorescent Cys probe SiR was developed by employing a novel "lock and key" strategy, which allows Cys to be detected without any interference or probe consumption caused by the intracellular high concentration of glutathione (GSH). Using SiR, we confirmed that inhibiting cystine (Cys2) transporter system xc - to deplete intracellular Cys is more efficient than inhibiting glutamate-cysteine ligase GCL to deplete intracellular GSH for sensitizing cancer cells to chemotherapy. Moreover, with the probe, a possible self-protection mechanism of cancer cells was indicated: when extracellular Cys sources are blocked, cancer cells could still survive by multidrug resistance protein transporter (Mrp1)-mediated export of intracellular GSH/GSSG as sources to supply intracellular Cys for resisting detrimental oxidative stress. Based on this finding, we further confirmed that abrogating the self-protection mechanism is an even more efficient strategy for sensitizing cancer cells to chemotherapy.
Keyphrases
- living cells
- fluorescent probe
- reactive oxygen species
- oxidative stress
- papillary thyroid
- signaling pathway
- drinking water
- quantum dots
- locally advanced
- squamous cell
- single molecule
- dna damage
- squamous cell carcinoma
- childhood cancer
- endoplasmic reticulum stress
- amino acid
- rectal cancer
- protein protein
- diabetic rats