Literature DB >> 24485302

Phylogeny, regeneration, ageing and cancer: role of microenvironment and possibility of its therapeutic manipulation.

K Smetana1, B Dvořánková1, L Lacina1.   

Abstract

Data about the possible correlation between reduction of the regeneration capacity in the course of phylogeny and formation of malignant tumours have been summarized from invertebrates to mammals. The evolutionarily increasing complexity of body building plane and expectancy of longevity in the course of phylogeny seems to be grossly negatively correlated with diminished regeneration capacity, but positively with increased occurrence of malignant tumours. A certain evolution-based switch-off mechanism reducing the extent of regeneration in developmentally complicated and long-living animals such as mammals and birds can be hypothesized and benefits of loss of this ability are discussed. This high incidence of malignancies seems to be related, in addition to other factors, to prolonged and cumulative exposure to cancerogenic stimuli in the course of lifetime. Longevity, supported by the progress and availability of medical care to the population, has been unveiling this phenomenon during recent decades. From this point of view, ageing represents the main risk for cancer acquisition. The probable role of microenvironment in all the discussed phenomena such as healing/regeneration, inflammation, and cancer is discussed and targeting of microenvironment is consequently predicted as a possible therapeutic target where controlled manipulation may represent a new approach to the treatment of cancer patients.

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Year:  2013        PMID: 24485302

Source DB:  PubMed          Journal:  Folia Biol (Praha)        ISSN: 0015-5500            Impact factor:   0.906


  3 in total

1.  Fibroblasts potentiate melanoma cells in vitro invasiveness induced by UV-irradiated keratinocytes.

Authors:  Njainday Pulo Jobe; Veronika Živicová; Alžběta Mifková; Daniel Rösel; Barbora Dvořánková; Ondřej Kodet; Hynek Strnad; Michal Kolář; Aleksi Šedo; Karel Smetana; Karolina Strnadová; Jan Brábek; Lukáš Lacina
Journal:  Histochem Cell Biol       Date:  2018-02-12       Impact factor: 4.304

2.  Cancer-associated fibroblasts are not formed from cancer cells by epithelial-to-mesenchymal transition in nu/nu mice.

Authors:  Barbora Dvořánková; Karel Smetana; Blanka Říhová; Jan Kučera; Rosana Mateu; Pavol Szabo
Journal:  Histochem Cell Biol       Date:  2014-11-12       Impact factor: 4.304

Review 3.  Cancer Microenvironment: What Can We Learn from the Stem Cell Niche.

Authors:  Lukas Lacina; Jan Plzak; Ondrej Kodet; Pavol Szabo; Martin Chovanec; Barbora Dvorankova; Karel Smetana
Journal:  Int J Mol Sci       Date:  2015-10-12       Impact factor: 5.923

  3 in total

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