Modulation of stress and immune response by Amblyomin-X results in tumor cell death in a horse melanoma model
Lichtenstein, Flavio ; Iqbal, Asif ; Will, Sonia Elisabete Alves de Lima ; Bosch, Rosemary Viola ; De Ocesano-Pereira, Carlos ; Goldfeder, Mauricio Barbugiani ; Chammas, Roger; Trufen, Carlos Eduardo Madureira ; Morais, Kátia Luciano Pereira ; Souza, Jean Gabriel de ; Natalino, Renato Jose Mendonça; Junqueira-de-Azevedo, Inácio de Loiola Meirelles ; Nishiyama Junior, Milton Yutaka ; Oliveira, Ursula Castro de ; Alves, Francisco Ivanio Arruda ; Araujo, Jaqueline Mayara de ; Lobba, Aline Ramos Maia ; Chudzinski-Tavassi, Ana Marisa
We have investigated Amblyomin-X-treated horse melanomas to better understand its mode of action through transcriptome analysis and the in vivo model. Amblyomin-X is a Kunitz-type homologous protein that selectively leads to the death of tumor cells via ER stress and apoptosis, currently under investigation as a new drug candidate for cancer treatment. Melanomas are immunogenic tumors, and a better understanding of the immune responses is warranted. Equine melanomas are spontaneous and not so aggressive as human melanomas are, as this study shows that the in vivo treatment of encapsulated horse melanoma tumors led to a significant reduction in the tumor size or even the complete disappearance of the tumor mass through intratumoral injections of Amblyomin-X. Transcriptome analysis identified ER- and mitochondria-stress, modulation of the innate immune system, apoptosis, and possibly immunogenic cell death activation. Interactome analysis showed that Amblyomin-X potentially interacts with key elements found in transcriptomics. Taken together, Amblyomin-X modulated the tumor immune microenvironment in different ways, at least contributing to induce tumor cell death.
Lichtenstein F, Iqbal A, Will SEAL, Bosch RV, De Ocesano-Pereira C, Goldfeder MB, et al. Modulation of stress and immune response by Amblyomin-X results in tumor cell death in a horse melanoma model. Sci. Rep.. 2020 Apr;10:6388. doi:10.1038/s41598-020-63275-2.
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