Abstract
Arsenic (As3+), a metalloid abundant in environment, is classified as a group I carcinogen associated with several common human cancers, including cancers in lung, skin, bladder, liver, and prostate (Wei et al., 2019). The mechanisms of As3+-induced carcinogenesis had been extensively studied, and different mechanisms might be involved in different types of cancer (Wei et al., 2019). Recent studies showed that exposure to a high dose of arsenic is able to induce lung cancer. Meanwhile, prolonged exposure to a low concentration of arsenic can increase the risk of lung cancer also (Liao et al., 2009; Fernández et al., 2012). Emerging evidence indicated that prolonged exposure to arsenic promotes malignant transformation and some of the transformed cells have cancer-stem-like properties (Ngalame et al., 2014). In the present report, we revealed that exposure to As3+ for short time period inhibited tyrosine-705 phosphorylation of signal transducer and activator of transcription 3 (pSTAT3Y705) and induced Src homology region 2 domain-containing phosphatase-1 (SHP-1) in bronchial epithelial cell line, BEAS-2B. In addition, we found that long term exposure of the cells to As3+ activates phosphorylation of STAT3 at serine 727 (pSTAT3S727) as well as pSTAT3Y705. Moreover, As3+ is able to induce the expression of miRNA-21 (miR-21) and decrease the expression of PDCD4. Taken together, our data suggest that activation of STAT3 and induction of miR-21 are important contributing factors to the reduced expression of PDCD4, which may play significant role in As3+-induced transformation of BEAS-2B cells.
•Short-term treatment of the BEAS-2B cells with arsenic induces pSTAT3S727 but inhibits pSTAT3Y705;•Long-term treatment of the BEAS-2B cells with arsenic induces both pSTAT3S727 and pSTAT3Y705;•Short-term arsenic treatment stabilizes SHP-1 protein, a tyrosine phosphatase negatively regulating pSTAT3Y705;•Sustained inhibition of SHP-1 in arsenic-transformed cells contributes to the activation of both pSTAT3S727 and pSTAT3Y705;•Arsenic induces miRNA-21, an oncogenic miRNA targeting tumor suppressor PDCD4, is partially dependent on STAT3 activation.