This medicine is also sometimes given off-label to help the following conditions: Also, let your doctor know if you drink large amounts of alcohol before starting on this medicine. Your doctor will probably want to order frequent tests to check your body's response to chloroquine. Chloroquine pharmacology Chloroquine toxicity cells Hydroxychloroquine plaquenil american college of rheumatology Jun 15, 2014 Moreover, elevated p62 is significantly correlated with poor survival in breast cancer patients Supplementary Figure 1, suggesting a role for autophagy in breast cancer reoccurrence 14-18. HCQ is a lysotropic chloroquine derivative that accumulates within lysosomes, resulting in lysosome neutralization and the inhibition of autophagic flux. Chloroquine, an antimalarial drug, inhibits autophagy by preventing degradation of autolysosomes. Moreover, chloroquine derivatives, such as hydroxychloroquine HCQ, in combination with antineoplastic chemotherapeutic drugs or radiotherapy treatments inhibit multiple cancer cell types. Phospho-SQSTM1/p62 Thr269/Ser272 Antibody recognizes endogenous levels of SQSTM1 protein only when phosphorylated at Thr269 and Ser272. This antibody may react with either dually or singly phosphorylated SQSTM1/p62. A background band is detected at 75 kDa in some cell lines. Species Reactivity Human, Mouse, Rat Let your healthcare provider know if your symptoms either don't improve or worsen while taking this medicine. Keep all appointments with your doctor and laboratory. P62 chloroquine Chloroquine Indications, Side Effects, Warnings -, Chloroquine Inhibits Autophagy to Potentiate Antiestrogen. Cheap aralen phosphateChloroquine toxicity treatment Chloroquine is the generic form of the brand-name prescription medicine Aralen, which is used to prevent and treat malaria — a mosquito-borne disease caused by a parasite — and to treat. Chloroquine Aralen - Side Effects, Dosage, Interactions.. CST - Phospho-SQSTM1/p62 Thr269/Ser272 Antibody. What does increasing both LC3 II and p62 mean?. NF-κB Signaling Activation Induced by Chloroquine Requires Autophagosome, p62 Protein, and c-Jun N-terminal Kinase JNK Signaling and Promotes Tumor Cell Resistance* Chloroquine is an anti-malaria medicine that works by interfering with the growth of parasites in the red blood cells of the human body. Parasites that cause malaria typically enter the body through the bite of a mosquito. Malaria is common in areas such as Africa, South America, and Southern Asia. In agreement, blocking lysosomal degradation using chloroquine CQ rescued LC3-II and p62 breakdown. Interestingly, caspase inhibition by ZVAD-fmk also increased the level of LC3-II and p62, suggesting that caspase signaling may modulate the autophagic process Figure 4D.