The presence of ROS is a constant feature in living cells metabolizing O2. ROS concentration and compartmentation determine their physiological or pathological effects. ROS overproduction is a feature of cancer cells and plays several roles during the natural history of malignant tumor. ROS continuously contribute to each step of cancerogenesis, from the initiation to the malignant progression, acting directly or indirectly. In this review, we will (a) underline the role of ROS in the pathway leading a normal cell to tumor transformation and progression, (b) define the multiple roles of ROS during the natural history of a tumor, (c) conciliate many conflicting data about harmful or beneficial effects of ROS, (d) rethink the importance of oncogene and tumor suppressor gene mutations in relation to the malignant progression, and (e) collocate all the cancer hallmarks in a mechanistic sequence which could represent a "physiological" response to the initial growth of a transformed stem/pluripotent cell, defining also the role of ROS in each hallmark. We will provide a simplified sketch about the relationships between ROS and cancer. The attention will be focused on the contribution of ROS to the signaling of HIF, NFκB, and Sirtuins as a leitmotif of cancer initiation and progressio

The interplay of reactive oxygen species, hypoxia, inflammation, and sirtuins in cancer initiation and progression / Tafani, Marco; Sansone, Luigi; Limana, Federica; Arcangeli, Tania; DE SANTIS, Elena; Polese, Milena; Massimo, Fini; Matteo, A. Russo3. - In: OXIDATIVE MEDICINE AND CELLULAR LONGEVITY. - ISSN 1942-0900. - STAMPA. - 2016:(2016). [10.1155/2016/3907147]

The interplay of reactive oxygen species, hypoxia, inflammation, and sirtuins in cancer initiation and progression

TAFANI, MARCO;SANSONE, LUIGI;LIMANA, FEDERICA;ARCANGELI, TANIA;DE SANTIS, Elena;POLESE, MILENA;
2016

Abstract

The presence of ROS is a constant feature in living cells metabolizing O2. ROS concentration and compartmentation determine their physiological or pathological effects. ROS overproduction is a feature of cancer cells and plays several roles during the natural history of malignant tumor. ROS continuously contribute to each step of cancerogenesis, from the initiation to the malignant progression, acting directly or indirectly. In this review, we will (a) underline the role of ROS in the pathway leading a normal cell to tumor transformation and progression, (b) define the multiple roles of ROS during the natural history of a tumor, (c) conciliate many conflicting data about harmful or beneficial effects of ROS, (d) rethink the importance of oncogene and tumor suppressor gene mutations in relation to the malignant progression, and (e) collocate all the cancer hallmarks in a mechanistic sequence which could represent a "physiological" response to the initial growth of a transformed stem/pluripotent cell, defining also the role of ROS in each hallmark. We will provide a simplified sketch about the relationships between ROS and cancer. The attention will be focused on the contribution of ROS to the signaling of HIF, NFκB, and Sirtuins as a leitmotif of cancer initiation and progressio
2016
reactive oxygen species; hypoxia; inflammation; sirtiuns; cancer
01 Pubblicazione su rivista::01a Articolo in rivista
The interplay of reactive oxygen species, hypoxia, inflammation, and sirtuins in cancer initiation and progression / Tafani, Marco; Sansone, Luigi; Limana, Federica; Arcangeli, Tania; DE SANTIS, Elena; Polese, Milena; Massimo, Fini; Matteo, A. Russo3. - In: OXIDATIVE MEDICINE AND CELLULAR LONGEVITY. - ISSN 1942-0900. - STAMPA. - 2016:(2016). [10.1155/2016/3907147]
File allegati a questo prodotto
File Dimensione Formato  
Tafani_Interplay_2016.pdf

accesso aperto

Note: Articolo principale
Tipologia: Altro materiale allegato
Licenza: Creative commons
Dimensione 3.09 MB
Formato Adobe PDF
3.09 MB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/847952
Citazioni
  • ???jsp.display-item.citation.pmc??? 158
  • Scopus 281
  • ???jsp.display-item.citation.isi??? 236
social impact