Abstract
BackgroundHypoxia-inducible factor 1 alpha (HIF-1α) is involved in processes promoting carcinogenesis of many tumors. However, its role in the development of colorectal cancer is unknown. To investigate the significance of HIF-1α during colorectal carcinogenesis and progression we examined its expression in precursor lesions constituting the conventional and serrated pathways, as well as in non-metastatic and metastatic adenocarcinomas.MethodsImmunohistochemistry and Western blot is used to analyse HIF-1α expression in normal colonic mucosa, hyperplastic polyps (HPP), sessile serrated adenomas (SSA), low-grade (TA-LGD) and high-grade (TA-HGD) traditional adenomas as well as in non-metastatic and metastatic colorectal adenocarcinomas. Eight colorectal carcinoma cell lines are tested for their HIF-1α inducibility after lipopolysaccharide (LPS) stimulation using western blot and immunocytochemistry.ResultsIn normal mucosa, HPP and TA-LGD HIF-1α was not expressed. In contast, perinuclear protein accumulation and nuclear expression of HIF-1α were shown in half of the examined SSA and TA-HGD. In all investigated colorectal carcinomas a significant nuclear HIF-1α overexpression compared to the premalignant lesions was observed but a significant correlation with the metastatic status was not found. Nuclear HIF-1α expression was strongly accumulated in perinecrotic regions. In these cases HIF-1α activation was seen in viable cohesive tumor epithelia surrounding necrosis and in dissociated tumor cells, which subsequently die. Enhanced distribution of HIF-1α was also seen in periiflammatory regions. In additional in vitro studies, treatment of diverse colorectal carcinoma cell lines with the potent pro-inflammatory factor lipopolysaccharide (LPS) led to HIF-1α expression and nuclear translocation.ConclusionWe conclude that HIF-1α expression occurs in early stages of colorectal carcinogenesis and achieves a maximum in the invasive stage independent of the metastatic status. Perinecrotic activation of HIF-1α in invasive tumors underlines a dual role of HIF-1α by regulating both pro-survival and pro-death processes. HIF-1α up-regulation in response to LPS-mediated stimulation and periinflammatory expression in invasive carcinomas suggest its involvement in inflammatory events. These patterns of HIF-1α inducibility could contribute indirectly to the acquisition of a metastatic phenotype.
Highlights
Hypoxia-inducible factor 1 alpha (HIF-1α) is involved in processes promoting carcinogenesis of many tumors
In the serrated pathway the histopathological sequence begins with the hyperplastic polyp (HP) without malignant potential, followed by the sessile serrated adenoma (SSA), recognised as a precursor lesion
In an in vitro study we recently reported that HIF-1α upregulation in response to hypoxia was accompanied by a significantly increased production of vascular endothelial growth factor (VEGF) in two of five colorectal carcinoma cell lines [47]
Summary
Hypoxia-inducible factor 1 alpha (HIF-1α) is involved in processes promoting carcinogenesis of many tumors. To investigate the significance of HIF-1α during colorectal carcinogenesis and progression we examined its expression in precursor lesions constituting the conventional and serrated pathways, as well as in nonmetastatic and metastatic adenocarcinomas. Hypoxia inducible factor 1 (HIF-1) is a transcription complex that plays a crucial role in coordinating the cellular response to oxygen stress conditions [3]. As a result of hypoxic stress, HIF-1 activates the transcription of a variety of genes regulating cell survival. Hypoxia leads to HIF-1α stabilization, resulting in a translocation of HIF-1α to the nucleus and binding to HIF-1β forming the active HIF-1 complex. The role of HIF-1α in tumor progression of colorectal carcinomas is still unclear and the published data so far are controversial. The expression of HIF-1α in some studies was correlated with an increased tumor aggressiveness, whereas in other studies a direct contribution to tumor progression was not found
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