AI Article Synopsis

  • * Researchers employed clinical analysis of placentas and sera, in vitro studies on tumor growth, and in vivo mouse models to study NLRP7's impact on CC.
  • * Findings revealed that NLRP7 promotes tumor cell proliferation and organization, while its absence in pregnant mice led to stronger maternal immune responses and reduced tumor growth and metastasis, highlighting its role in creating an immunosuppressive environment that aids CC progression.

Article Abstract

The inflammatory gene is the major gene responsible for recurrent complete hydatidiform moles (CHM), an abnormal pregnancy that can develop into gestational choriocarcinoma (CC). However, the role of NLRP7 in the development and immune tolerance of CC has not been investigated. Three approaches were employed to define the role of NLRP7 in CC development: (i) a clinical study that analyzed human placenta and sera collected from women with normal pregnancies, CHM or CC; (ii) an in vitro study that investigated the impact of NLRP7 knockdown on tumor growth and organization; and (iii) an in vivo study that used two CC mouse models, including an orthotopic model. NLRP7 and circulating inflammatory cytokines were upregulated in tumor cells and in CHM and CC. In tumor cells, NLRP7 functions in an inflammasome-independent manner and promoted their proliferation and 3D organization. Gravid mice placentas injected with CC cells invalidated for , exhibited higher maternal immune response, developed smaller tumors, and displayed less metastases. Our data characterized the critical role of NLRP7 in CC and provided evidence of its contribution to the development of an immunosuppressive maternal microenvironment that not only downregulates the maternal immune response but also fosters the growth and progression of CC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232770PMC
http://dx.doi.org/10.3390/cancers13122999DOI Listing

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