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Exploring the links between cancer and placenta development.

Vincenzo Costanzo1,2, Alberto Bardelli3,4, Salvatore Siena2,5

  • 1IFOM, The FIRC Institute of Molecular Oncology, University of Milan Medical School, Milan, Italy vincenzo.costanzo@ifom.eu.

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Cancer cells mimic placental development to invade tissues and evade immune responses. Understanding this link could improve immunotherapies and DNA damage treatments for metastatic cancer.

Keywords:
DNA damage responseDNA repaircancer

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Area of Science:

  • Oncology
  • Developmental Biology
  • Immunology

Background:

  • Metastatic cancer development is a lengthy, multistage process.
  • Genetic instability in cancer precursors leads to heterogeneous cell populations.
  • Despite heterogeneity, cancers exhibit stereotypical behaviors like invasiveness and immune suppression.

Purpose of the Study:

  • To investigate the poorly understood mechanisms behind stereotypical cancer properties.
  • To explore the potential link between embryonic development reactivation and immune response modulation in cancer.
  • To understand how genotoxic stress promotes cancer via early mammalian placentation programs.

Main Methods:

  • Comparative analysis of molecular and cellular mechanisms in embryonic development and cancer.
  • Investigation of immune evasion strategies employed by trophoblast cells and tumor cells.
  • Exploration of neo-antigen generation in embryos and tumors.

Main Results:

  • Tumors and embryos share the need to avoid immune responses.
  • Trophoblast cells, crucial for embryonic development, exhibit malignant features like invasion and immune evasion.
  • Both trophoblast and tumor cells utilize cancer immunoediting strategies.

Conclusions:

  • Reactivation of embryonic development programs in genetically unstable cells may drive tumor expansion and metastasis.
  • Understanding the parallels between placentation and cancer progression can clarify resistance to current therapies.
  • This knowledge may lead to novel therapeutic strategies for cancer eradication.