179
Views
3
CrossRef citations to date
0
Altmetric
Original Articles

Morphological features of pulmonary fibrosis in workers occupationally exposed to alpha radiation

, , , , &
Pages 448-460 | Received 25 Jul 2019, Accepted 16 Dec 2019, Published online: 06 Feb 2020

References

  • Allen DC, Cameron RI, editors. 2013. Histopathology specimens. Clinical, pathological and laboratory aspects. 2nd ed. Berlin (Germany): Springer.
  • Almeida C, Nagarajan D, Tian J, Leal SW, Wheeler K, Munley M, Blackstock W, Zhao W. 2013. The role of alveolar epithelium in radiation-induced lung injury. PLoS One. 8(1):e53628.
  • Ashcroft T, Simpson JM, Timbrell V. 1988. Simple method of estimating severity of pulmonary fibrosis on a numerical scale. J Clin Pathol. 41(4):467–470.
  • Azizova TV, Bannikova MV, Grigoryeva ES, Rybkina VL. 2018. Risk of malignant skin neoplasms in a cohort of workers occupationally exposed to ionizing radiation at low dose rates. PLoS One. 13(10):e0205060.
  • Azizova TV, Bannikova MV, Zhuntova GV, Grigoryeva ES, Moseeva MB, Bragin EV. 2019. Registry for chronic radiation syndrome in a worker cohort of the Russian nuclear enterprise, the Mayak production association. J Radiol Prot. 39(3):890–905.
  • Azizova T, Briks K, Bannikova M, Grigoryeva E. 2019. Hypertension incidence risk in a cohort of Russian workers exposed to radiation at the Mayak production association over prolonged periods. Hypertension. 73(6):1174–1184.
  • Azizova TV, Day RD, Wald N, Muirhead CR, Oʼhagan JA, Sumina MV, Belyaeva ZD, Druzhinina MB, Teplyakov II, Semenikhina NG, et al. 2008. The “clinic” medical-dosimetric database of Mayak production association workers: structure, characteristics and prospects of utilization. Health Phys. 94(5):449–458.
  • Azizova TV, Grigoryeva ES, Haylock RGE, Pikulina MV, Moseeva MB. 2015. Ischaemic heart disease incidence and mortality in an extended cohort of Mayak workers first employed in 1948–1982. Br J Radiol. 88(1054):20150169.
  • Azizova TV, Moseeva MB, Grigoryeva ES, Zhuntova GV, Bannikova MV, Sychugov GV, Kazachkov EL. 2020. Registry of plutonium-induced lung fibrosis in a Russian nuclear worker cohort. Health Phys. 118:185–192.
  • Azizova TV, Zhuntova GV, Haylock RGE, Moseeva MB, Grigoryeva ES, Bannikova MV, Belyaeva ZD, Bragin EV. 2017. Chronic bronchitis incidence in the extended cohort of Mayak workers first employed during 1948–1982. Occup Environ Med. 74(2):105–113.
  • Bentzen SM, Skoczylas JZ, Bernier J. 2000. Quantitative clinical radiobiology of early and late lung reactions. Int J Radiat Biol. 76(4):453–462.
  • Brooks AL, Guilmette RA, Hahn FF, Haley PJ, Muggenburg BA, Mewhinney JA, McClellan RO. 1992. Distribution and biological effects of inhaled 239 Pu(NO3) 4 in cynomolgus monkeys. Radiat Res. 130(1):79–87.
  • Burgstaller G, Oehrle B, Gerckens M, White ES, Schiller HB, Eickelberg O. 2017. The instructive extracellular matrix of the lung: basic composition and alterations in chronic lung disease. Eur Respir J. 50(1):1601805.
  • Chen FP, Gong LK, Zhang L, Wang H, Qi XM, Wu XF, Xiao Y, Cai Y, Liu LI, Li XH, Ren J. 2007. Early lung injury contributes to lung fibrosis via AT1 receptor in rats. Acta Pharmacol Sin. 28(2):227–237.
  • Coggle JE, Lambert BE, Moores SR. 1986. Radiation effects in the lung. Environ Health Perspect. 70:261–291.
  • Désogère P, Tapias LF, Hariri LP, Rotile NJ, Rietz TA, Probst CK, Blasi F, Day H, Mino-Kenudson M, Weinreb P, et al. 2017. Type I collagen-targeted PET probe for pulmonary fibrosis detection and staging in preclinical models. Sci Transl Med. 9(384):eaaf4696.
  • Doschenko VN, Kislovskaya IL, Lemberg VK, Nifatov AP. 1967. Clinical and morphological characteristics of plutonium-induced pulmonary fibrosis. Bull Radiat Med. 3:32–46.
  • Dunsmore SE. 2008. Treatment of COPD: a matrix perspective. Int J Chron Obstruct Pulmon Dis. 3(1):113–122.
  • Flechsig P, Dadrich M, Bickelhaupt S, Jenne J, Hauser K, Timke C, Peschke P, Hahn EW, Grone HJ, Yingling J, et al. 2012. LY2109761 attenuates radiation‐induced pulmonary murine fibrosis via reversal of TGF‐beta and BMP‐associated proinflammatory and proangiogenic signals. Clin Cancer Res. 18(13):3616–3627.
  • Fountos BN. 2017. The department of energy’s Russian health studies program. Radiat Prot Dosimetry. 176(1–2):3–521.
  • Fyfe B, Miller DV, editors. 2016. Diagnostic pathology: hospital autopsy. 1st ed. Philadelphia (PA): Elsevier; p. 106.
  • Gilbert ES, Schonfeld SJ, Sokolnikov ME, Schadilov AE, Vasilenko EK, Koshurnikova NA, Preston DL. 2013. Lung cancer risks from plutonium: an updated analysis of data from the Mayak worker cohort. Radiat Res. 179(3):332–342.
  • Gilhodes JC, Jule Y, Kreuz S, Stierstorfer B, Stiller B, Wollin L. 2017. Quantification of pulmonary fibrosis in a Bleomycin mouse model using automated histological image analysis. PLoS One. 12(1):e0170561.
  • Guskova AK, Baisogolov GD. 1971a. Human radiation syndrome (sketches). Moscow (Russia): Medicine.
  • Guskova AK, Baisogolov GD. 1971b. Radiation sickness in man (outlines). New York (NY): United Nations.
  • Hahn FF, Romanov SA, Guilmette RA, Nifatov AP, Zaytseva YV, Diel JH, Allen SW, Lyovkina YV. 2003. Distribution of plutonium particles in the lungs of Mayak workers. Radiat Prot Dosimetry. 105(1–4):81–84.
  • Hubner RH, Gitter W, El Mokhtari NE, Mathiak M, Both M, Bolte H, Freitag-Wolf S, Bewig B. 2008. Standardized quantification of lung fibrosis in histological samples. Biotechniques. 44:507–517.
  • Ilyin LA, editor. 2005. Plutonium. Radiation safety. Moscow: IzdAT; p. 416.
  • International Commission on Radiological Protection. 1993. Age-dependent doses to members of the public from intake of radionuclides, Part 2. ICRP publication 67. Oxford: Pergamon Press; p. 167.
  • International Commission on Radiological Protection. 2012. Statement on tissue reactions and early and late effects of radiation in normal tissues and organs – threshold doses for tissue reactions in a radiation protection context. ICRP Publication 118. Ann ICRP. 41(1/2):1–322.
  • Jones MG, Andriotis OG, Roberts JJ, Lunn K, Tear VJ, Cao L, Ask K, Smart DE, Bonfanti A, Johnson P, et al. 2018. Nanoscale dysregulation of collagen structure-function disrupts mechano-homeostasis and mediates pulmonary fibrosis. eLife. 7:e36354.
  • Kim KK, Kugler MC, Wolters PJ, Robillard L, Galvez MG, Brumwell AN, Sheppard D, Chapman HA. 2006. Alveolar epithelial cell mesenchymal transition develops in vivo during pulmonary fibrosis and is regulated by the extracellular matrix. Proc Natl Acad Sci USA. 103(35):13180–13185.
  • Kobayashi T, Gabazza EC, Taguchi O, Risteli J, Risteli L, Kobayashi H, Yasui H, Yuda H, Sakai T, Kaneda M, et al. 1999. Type I collagen metabolites as tumor markers in patients with lung carcinoma. Cancer. 85(9):1951–1957.
  • Koshurnikova NA, Aristov VP, Lemberg VK, Mushkacheva GS, Poplyko MG, Tseveleva IA. 1972. Mechanisms of development of plutonium-induced pulmonary sclerosis. Health Phys. 22(6):753–754.
  • Koshurnikova NA, Sokolnikov ME, Fomin EP. 2014. Excess relative lung cancer risk depending on the histological type of the tumor. J Radiat Saf Issue. 4(76):62–69.
  • Kruglov A. 2002. The history of the soviet atomic industry. London: Taylor and Francis; p. 288.
  • Lawson CL, Hanson RJ. 1996. Solving least squares problems. Revised republication. Philadelphia (PA): Society for Industrial and Applied Mathematics; p. 352.
  • Loffredo C, Goerlitz D, Sokolova S, Leondaridis L, Zakharova M, Revina V, Kirillova E. 2017. The Russian human tissue radiobiological tissue repository: a unique resources for studies of plutonium-exposed workers. Radiat Prot Dosimetry. 173(1–3):10–15.
  • Madri JA, Furthmayr H. 1980. Collagen polymorphism in the lung. An immunochemical study of pulmonary fibrosis. Hum Pathol. 11(4):353–366.
  • Mak KM, Png CY, Lee DJ. 2016. Type V collagen in health, disease, and fibrosis. Anat Rec (Hoboken). 299(5):613–629.
  • McDonald S, Rubin P, Phillips TL, Marks LB. 1995. Injury to the lung from cancer therapy: clinical syndromes, measurable endpoints, and potential scoring systems. Int J Radiat Oncol Biol Phys. 31(5):1187–1203.
  • Napier BA. 2017. The Mayak worker dosimetry system (MWDS-2013): an introduction to the socumentation. Radiat Prot Dosimetry. 176(1–2):6–9.
  • O’Dwyer DN, Moore BB. 2017. The role of periostin in lung fibrosis and airway remodeling. Cell Mol Life Sci. 74(23):4305–4314.
  • Padgett WJ. 2011. Weibull distribution. In: Lovric M, editors. International encyclopedia of statistical science. Berlin (Heidelberg): Springer.
  • Park JF, Watson CR, Buschbom RL, Dagle GE, Strom DJ, Weller RE. 2012. Biological effects of inhaled 239PuO2 in beagles. Radit Res. 178(5):447–467.
  • Parra ER, Aguiar AC, Jr, Teodoro WR, de Souza R, Yoshinari NH, Capelozzi VL. 2009. Collagen V and vascular injury promote lung architectural changes in systemic sclerosis. Clin Respir J. 3(3):135–142.
  • Polette M, Thiblet J, Ploton D, Buisson AS, Monboisse JC, Tournier JM, Birembaut P. 1997. Distribution of a1(IV) and a3(IV) chains of type IV collagen in lung tumours. J Pathol. 182(2):185–191.
  • Rydell-Törmänen K, Andreasson K, Hesselstrand R, Risteli J, Heinegård D, Saxne T, Westergren-Thorsson G. 2012. Extracellular matrix alterations and acute inflammation; developing in parallel during early induction of pulmonary fibrosis. Lab Invest. 92(6):917–925.
  • Sokolnikov ME, Gilbert ES, Preston DL, Ron E, Shilnikova NS, Khokhryakov VV, Vasilenko EK, Koshurnikova NA. 2008. Lung, liver and bone cancer mortality in Mayak workers. Int J Cancer. 123(4):905–911.
  • Suki B, Bates JH. 2008. Extracellular matrix mechanics in lung parenchymal diseases. Respir Physiol Neurobiol. 163(1–3):33–43.
  • Sullivan JA, Jankowska-Gan E, Hegde S, Pestrak MA, Agashe VV, Park AC, Brown ME, Kernien JF, Wilkes DS, Kaufman DB, et al. 2017. Th17 responses to collagen type V, kα1-tubulin, and vimentin are present early in human development and persist throughout life. Am J Transplant. 17(4):944–956.
  • Suvarna K, Layton C, Bancroft JD. 2018. Bancroft’s theory and practice of histological techniques. 8th ed. Amsterdam (Netherlands): Elsevier; p. 672.
  • Sychugov GV, Kazachkov EL, Azizova TV, Teplyakova OV, Revina VS. 2014. Immunomorphological characteristics of pneumofibrosis at workers of plutonium manufacture. Ural Med J. Pathomorphology. 8(122):71–76.
  • Tabata C, Kadokawa Y, Tabata R, Takahashi M, Okoshi K, Sakai Y, Mishima M, Kubo H. 2006. All-trans-retinoic acid prevents radiation- or bleomycin-induced pulmonary fibrosis. Am J Respir Crit Care Med. 174(12):1352–1360.
  • Togari H, Hashimoto Y, Wada Y, Hayakawa T. 1993. Increased type III/I collagen and α1(I)/α2(I) chain in a bronchopulmonary dysplastic lung. Pediatr Int. 35(2):101–107.
  • Tokarskaya ZB, Okladnikova ND, Belyaeva ZD, Drozhko EG. 1995. The influence of radiation and nonradiation factors on the lung cancer incidence among the workers of the nuclear enterprise Mayak. Health Phys. 69(3):356–366.
  • Urawa M, Kobayashi T, D’Alessandro-Gabazza CN, Fujimoto H, Toda M, Roeen Z, Hinneh JA, Yasuma T, Takei Y, Taguchi O, et al. 2016. Protein S is protective in pulmonary fibrosis. J Thromb Haemost. 14(8):1588–1599.
  • van Der Meeren A, Gremy O, Renault D, Miroux A, Bruel S, Griffiths N, Tourdes F. 2012. Plutonium behavior after pulmonary administration according to solubility properties and consequences on alveolar macrophage activation. J Radiat Res. 53(2):184–194.
  • Volkova LG. 1961. Pneumosclerosis as an outcome of radiation diseases induced by plutonium intoxication. Bull Radiat Med. 2:82–91.
  • Yoshida S, Haque A, Mizobuchi T, Iwata T, Chiyo M, Webb TJ, Baldridge LA, Heidler KM, Cummings OW, Fujisawa T, et al. 2006. Anti-type V collagen lymphocytes that express IL-17 and IL-23 induce rejection pathology in fresh and well-healed lung transplants. Am J Transplant. 6(4):724–735.
  • Zar JH. 1999. Biostatistical analysis. Upper Saddle River (NJ): Prentice Hall.
  • Zhou C, Moustafa MR, Cao L, Kriegsmann M, Winter M, Schwager C, Jones B, Wang S, Bauerle T, Zhou PK, et al. 2019. Modeling and multiscale characterization of the quantitative I, aging based fibrosis index reveals pathophysiological, transcriptome and proteomic correlates of lung fibrosis induces by fractionated irradiation. Int J Cancer. 144(12):3160–3173.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.