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Emergency myelopoiesis in solid cancers.
Aliazis, Konstantinos; Yenyuwadee, Sasitorn; Phikulsod, Ployploen; Boussiotis, Vassiliki A.
Afiliação
  • Aliazis K; Department of Hematology-Oncology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Yenyuwadee S; Department of Hematology-Oncology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Phikulsod P; Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Boussiotis VA; Division of Hematology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Br J Haematol ; 2024 Jul 23.
Article em En | MEDLINE | ID: mdl-39044285
ABSTRACT
Cells of the innate and adaptive immune systems are the progeny of haematopoietic stem and progenitor cells (HSPCs). During steady-state myelopoiesis, HSPC undergo differentiation and proliferation but are called to respond directly and acutely to various signals that lead to emergency myelopoiesis, including bone marrow ablation, infections, and sterile inflammation. There is extensive evidence that many solid tumours have the potential to secrete classical myelopoiesis-promoting growth factors and other products able to mimic emergency haematopoiesis, and to aberrantly re-direct myeloid cell development into immunosuppressive cells with tumour promoting properties. Here, we summarize the current literature regarding the effects of solid cancers on HSPCs function and discuss how these effects might shape antitumour responses via a mechanism initiated at a site distal from the tumour microenvironment.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article