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“Nature” sub-issue: Why does the hypoxic microenvironment make the tumor extremely evil?
Why does the hypoxic microenvironment make the tumor extremely evil? Hypoxia or insufficient tissue oxygenation is a key factor that makes most cancers difficult to cure, and it also leads to increased drug resistance of cancer cells. Therefore, remodeling the immunosuppressive microenvironment of tumors has become a new challenge to improve immune efficacy.
Recently, researchers from the Research Group of Tumor Immunotherapy and Microenvironment (TIME) of the Luxembourg Institute of Health (LIH) published an article titled Targeting HIF-1 alpha transcriptional activity drives cytotoxic immune effector in the sub-issue of “Nature” “oncogene”. The article on cells into melanoma and improves combination immunotherapy, based on a gene editing technology, shows us how targeting HIF-1α can inhibit tumor growth and drive cytotoxic T lymphocytes (CTL) into tumor tissues.
As we all know, tumor hypoxia is mainly caused by the imbalance between the low oxygen supply caused by abnormal vascularization and the high oxygen consumption of tumor cells, and the rapid proliferation of tumor cells will accelerate the consumption of oxygen, thereby limiting the available for further spread to The amount of oxygen in the tumor tissue.
The main reason why cancer is difficult to cure is that tumor cells will continue to adapt to the bad environment. Hypoxia Inducible Factor-1α (Hypoxia Inducible Factor-1α) is widely present in mammals and humans under hypoxic conditions. The expression of a transcription factor is closely related to tumor proliferation, invasion and metastasis, tumor angiogenesis and other characteristics.
Studies have found that melanoma, as a highly deteriorating skin tumor, can not only survive in hypoxic environments by activating HIF-1α, but also can hijack important immune system signals and destroy the resistance of conventional anti-cancer therapies such as radiotherapy and chemotherapy. Sexual mechanism to give full play to their own advantages.
Therefore, in order to understand how cancer cells overcome the hypoxic environment in order to find effective anti-cancer therapies, the researchers specifically excised the HIF-1α/ARNT dimerization domain in mice based on the CRISPR gene editing technology. The effect of inhibiting HIF-1α transcriptional activity on tumor growth, immune cell infiltration and immunotherapy was evaluated in a preclinical mouse model of melanoma.
The results of the study showed that the expression of HIF-1α downstream target genes such as carbonic anhydrase 9 (Ca-9), glucose transporter-1 (Slc2a1) and vascular endothelial growth factor (Vegf) did not increase, indicating that the HIF-knockout 1α can effectively block its transcriptional activity in melanoma, and blocking the transcriptional activity of HIF-1α can effectively inhibit the growth of melanoma.
Moreover, the results of immunohistochemical (IHC) staining of tumor sections showed that there was no CA-9 staining in HIF-1α (Del) mice. In addition, the researchers also found that by increasing the release of the chemokine “CCL5”, it can promote the infiltration of immune cells such as NK and CD8+T into the tumor microenvironment and promote tumor regression.
More importantly, the researchers also evaluated the anti-tumor drug Acriflavine (ACF) combined with two immunotherapies (anti-PD-1 immune checkpoint blocking antibody and TRP peptide vaccine) for the treatment of melanoma. Surprisingly, the triple therapy (anti-PD-1 + TRP + ACF) can effectively inhibit tumor growth. This result more powerfully proves that targeting the relevant hypoxia pathway in the tumor microenvironment can improve the therapeutic effect of immunotherapy .
All in all, the research provides a valuable new anti-cancer target, bringing a new line of life to cancer patients, and at the same time, it provides strong preclinical evidence for a new combination of triple cancer treatment strategies.
(source:internet, reference only)