AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer

Abstract

Allogeneic inflammatory factor-1 (AIF-1) overexpression has been reported to be associated with tumorigenesis and tumor metastasis. This study aimed to investigate the role of AIF-1 in the development and progression of non-small cell lung cancer (NSCLC). AIF-1, IL-6, and VEGF expressions in human NSCLC tissue were examined by immunofluorescence staining. Bioinformatics analyses were performed to identify AIF-1-related molecules and pathways in NSCLC. Human lung cancer A549 cell proliferation was assessed by CCK-8 assay, and cell migration was evaluated with wound-healing assay. IL-6 and VEGF secretions in A549 cell culture supernatants were quantified using the Elecsys IL-6 immunoassay kit and Vascular Endothelial Growth Factor Assay Kit. RT-PCR and western blot were performed to quantify the expressions of AIF-1, IL-6, and VEGF mRNAs and proteins involved in p38-MAPK and JAK/STAT3 signaling such as p-p38 and p-STAT3. The effects of AIF-1 on A549 cell proliferation and the expressions of IL-6 and VEGF were assessed using SB203580 and ruxolitinib. The results showed that AIF-1 expression was higher in human NSCLC tissue than that in paracancer tissue. High AIF-1 expression was associated with metastasis, higher TNM stage, and poorer survival. Bioinformatics connected AIF-1 to JAK/STAT signaling in NSCLC. AIF-1 increased A549 cell proliferation, migration, IL-6 secretion and, VEGF secretion, and these effects were attenuated by inhibition of p38-MAPK or JAK/STAT3 signaling. In conclusion, AIF-1 may promote aggressive NSCLC behavior via activation of p38-MAPK and JAK/STAT signaling.

Prognostic Value of Histone Acetyl Transferase 1 (HAT-1) and Inflammatory Signatures in Pancreatic Cancer

“…This molecule orchestrates both immune (i.e., controlling proliferation, the migration and polarization of T lymphocytes, and the activation of macrophages or microglia or modulating dendritic cells) and non-immune actions (i.e., modulation of membrane ruffling, activation of endothelial cells, cell cycle progression and F-actin binding activity) [44]. The role of AIF-1 in cancer has been demonstrated in past works, mainly focused on hepatocellular carcinoma [45], breast [46], lung [47] and other types of cancer [48][49][50]. To our best knowledge, no studies have been conducted to understand the carcinogenic role and prognostic value of AIF-1 in pancreatic cancer; a recent study [51] revealed that AIF-1 acts as a robust diagnostic and prognostic biomarker in several types of cancer and is closely correlated with tumor immune infiltration.…”

AIF1: Function and Connection with Inflammatory Diseases

“…With respect to infantile hemangioma, AIF1 expression was found specifically in ECs, and the authors suggested that this EC-specific expression may trigger the recruitment of myeloid cells [140]. In non-small cell lung cancer (NSCLC), AIF1 expression was upregulated, and associated with metastasis, higher TNM stage, and poorer survival [141]. Moreover, AIF1 may promote this aggressive tumor function via the activation of p38-MAPK and JAK/STAT signaling.…”