4.1 Article

Damaging and protective bystander cross-talk between human lung cancer and normal cells after proton microbeam irradiation

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.mrfmmm.2014.03.004

Keywords

Proton microbeam; DNA double-strand breaks; gamma-H2AX; Bystander cross-talk; Gap junctional intercellular communication; Human lung cancer and normal fibroblast; cells

Funding

  1. DAE Graduate Fellowship Scheme
  2. Department of Atomic Energy, Government of India
  3. Homi Bhabha National Institute, Mumbai
  4. Centre for International Co-operation in Science (CICS), Chennai
  5. UICC-ICRETT [ICR/10/071]
  6. JSPS KAKENHI [25861137]
  7. NIRS-SPICE [513-PB01]
  8. Grants-in-Aid for Scientific Research [25861137] Funding Source: KAKEN

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Most of the studies of radiation-induced bystander effects (RIBE) have been focused on understanding the radiobiological changes observed in bystander cells in response to the signals from irradiated cells in a normal cell population with implications to radiation risk assessment. However, reports on RIBE with relevance to cancer radiotherapy especially investigating the bidirectional and criss-cross bystander communications between cancer and normal cells are limited. Hence, in present study employing co-culture approach, we have investigated the bystander cross-talk between lung cancer (A549) and normal (WI38) cells after proton-microbeam irradiation using gamma-H2AX foci fluorescence as a measure of DNA double-strand breaks (DSBs). We observed that in A549-A549 co-cultures, irradiated A549 cells exert damaging effects in bystander A549 cells, which were found to be mediated through gap junctional intercellular communication (GJIC). However, in A549-WI38 co-cultures, irradiated A549 did not affect bystander WI38 cells. Rather, bystander WI38 cells induced inverse protective signalling (rescue effect) in irradiated A549 cells, which was independent of GJIC. On the other hand, in response to irradiated WI38 cells neither of the bystander cells (A549 or WI38) showed significant increase in gamma-H2AX foci. The observed bystander signalling between tumour and normal cells may have potential implications in therapeutic outcome of cancer radiotherapy. (C) 2014 Elsevier B.V. All rights reserved.

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