| Literature DB >> 31655928 |
Emily Latacz1,2,3, Elisabetta Caspani2,3, Raymond Barnhill4,5, Claire Lugassy4, Cornelis Verhoef6, Dirk Grünhagen6, Steven Van Laere2,3, Carlos Fernández Moro7,8, Marco Gerling9,10, Marie Dirix11, Luc Y Dirix2, Peter B Vermeulen12,13.
Abstract
Cancer cells can use existing blood vessels to acquire a vasculature. This process is termed 'vessel co-option'. Vessel co-option is an alternative to the growth of new blood vessels, or angiogenesis, and is adopted by a wide range of human tumour types growing within numerous tissues. A complementary aspect of this process is extravascular migratory tumour spread using the co-opted blood vessels as a trail. Vessel co-opting tumours can be discriminated from angiogenic tumours by specific morphological features. These features give rise to distinct histopathological growth patterns that reflect the interaction of cancer cells with the microenvironment of the organ in which they thrive. We will discuss the histopathological growth patterns of vessel co-option in the brain, the liver and the lungs. The review will also highlight evidence for the potential clinical value of the histopathological growth patterns of cancer. Vessel co-option can affect patient outcomes and resistance to cancer treatment. Insight into the biological drivers of this process of tumour vascularization will yield novel therapeutic strategies.Entities:
Keywords: Angiogenesis; Angiotropism; Extravascular migratory metastasis; Histopathological growth patterns; Metastasis; Pericytic mimicry; Tumour microenvironment; Vessel co-option
Mesh:
Year: 2019 PMID: 31655928 DOI: 10.1007/s10456-019-09690-0
Source DB: PubMed Journal: Angiogenesis ISSN: 0969-6970 Impact factor: 9.596