AI Article Synopsis

  • * Researchers used siRNA to silence FBLN1 in MSM cell lines and examined its effects on apoptosis (cell death), proliferation (cell growth), and autophagy (cell recycling), discovering significant changes in gene expression related to these processes.
  • * The findings suggest that silencing FBLN1 promotes cell proliferation, indicating it may act as a tumor suppressor; thus, targeting FBLN1 could be a potential treatment strategy for advanced-stage MSM cancer. *

Article Abstract

Introduction: The impaired balance between cell proliferation and cell death, followed the inability to receive the death signals, cells push towards the neoplasia pathway. Fibulin 1 (FBLN1) plays a role as a co-factor in the mechanism of action of a protease such as a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS-1), which has important roles in angiogenesis, can also act as both tumor suppressor gene (TSG) and an oncogene in the main constituent of the extra-cellular matrix. This preliminary study has investigated the effects of silencing FBLN1 with siRNA on autophagy, proliferation, apoptosis pathways in the MSM cell line.

Material And Methods: It was transfected siRNA specific to FBLN1 incubated MSM SPC212 cells, and compared with negative control siRNAs by a real-time polymerase chain reaction. It was determined apoptosis, proliferation, autophagy-related genes in mRNA levels.

Results: It was observed that increased anti-apoptosis genes, such as , and , anti-apoptotic gene, reduced . Proliferation induced through while increased genes. Autophagy increased via increasing genes while decreased via suppressed , and genes by silencing FBLN1 with siRNAs ( < 0.05).

Conclusions: Proliferation can be induction with silencing of FBLN1 with siRNA in processing mechanism MSM. It was concluded that FBLN1 could be act as pleiotropic on autophagy, and apoptosis pathways in proliferation processing for MSM. Therefore we think that FBLN1 acts like a TSG. FBLN1 can be considered as a targeted treatment option in advanced stage MSM.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7836276PMC
http://dx.doi.org/10.5114/wo.2020.102826DOI Listing

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Article Synopsis
  • * Researchers used siRNA to silence FBLN1 in MSM cell lines and examined its effects on apoptosis (cell death), proliferation (cell growth), and autophagy (cell recycling), discovering significant changes in gene expression related to these processes.
  • * The findings suggest that silencing FBLN1 promotes cell proliferation, indicating it may act as a tumor suppressor; thus, targeting FBLN1 could be a potential treatment strategy for advanced-stage MSM cancer. *
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