| 1. |
- Aimonen, Kukka, et al.
(författare)
-
Role of Surface Chemistry in the In Vitro Lung Response to Nanofibrillated Cellulose
- 2021
-
Ingår i: Nanomaterials. - : MDPI. - 2079-4991. ; 11:2
-
Tidskriftsartikel (refereegranskat)abstract
- Wood-derived nanofibrillated cellulose (NFC) has emerged as a sustainable material with a wide range of applications and increasing presence in the market. Surface charges are introduced during the preparation of NFC to facilitate the defibrillation process, which may also alter the toxicological properties of NFC. In the present study, we examined the in vitro toxicity of NFCs with five surface chemistries: nonfunctionalized, carboxymethylated, phosphorylated, sulfoethylated, and hydroxypropyltrimethylammonium-substituted. The NFC samples were characterized for surface functional group density, surface charge, and fiber morphology. Fibril aggregates predominated in the nonfunctionalized NFC, while individual nanofibrils were observed in the functionalized NFCs. Differences in surface group density among the functionalized NFCs were reflected in the fiber thickness of these samples. In human bronchial epithelial (BEAS-2B) cells, all NFCs showed low cytotoxicity (CellTiter-GloVR luminescent cell viability assay) which never exceeded 10% at any exposure time. None of the NFCs induced genotoxic effects, as evaluated by the alkaline comet assay and the cytokinesis-block micronucleus assay. The nonfunctionalized and carboxymethylated NFCs were able to increase intracellular reactive oxygen species (ROS) formation (chloromethyl derivative of 2 ',7 '-dichlorodihydrofluorescein diacetate assay). However, ROS induction did not result in increased DNA or chromosome damage.
|
|
| 2. |
- Bonassi, Stefano, et al.
(författare)
-
An increased micronucleus frequency in peripheral blood lymphocytes predicts the risk of cancer in humans
- 2007
-
Ingår i: Carcinogenesis. - : Oxford University Press (OUP). - 0143-3334 .- 1460-2180. ; 28:3, s. 625-631
-
Tidskriftsartikel (refereegranskat)abstract
- The frequency of micronuclei (MN) in peripheral blood lymphocytes (PBL) is extensively used as a biomarker of chromosomal damage and genome stability in human populations. Much theoretical evidence has been accumulated supporting the causal role of MN induction in cancer development, although prospective cohort studies are needed to validate MN as a cancer risk biomarker. A total of 6718 subjects from of 10 countries, screened in 20 laboratories for MN frequency between 1980 and 2002 in ad hoc studies or routine cytogenetic surveillance, were selected from the database of the HUman MicroNucleus (HUMN) international collaborative project and followed up for cancer incidence or mortality. To standardize for the inter-laboratory variability subjects were classified according to the percentiles of MN distribution within each laboratory as low, medium or high frequency. A significant increase of all cancers incidence was found for subjects in the groups with medium (RR = 1.84; 95% CI: 1.28-2.66) and high MN frequency (RR = 1.53; 1.04-2.25). The same groups also showed a decreased cancer-free survival, i.e. P = 0.001 and P = 0.025, respectively. This association was present in all national cohorts and for all major cancer sites, especially urogenital (RR = 2.80; 1.17-6.73) and gastro-intestinal cancers (RR = 1.74; 1.01-4.71). The results from the present study provide preliminary evidence that MN frequency in PBL is a predictive biomarker of cancer risk within a population of healthy subjects. The current wide-spread use of the MN assay provides a valuable opportunity to apply this assay in the planning and validation of cancer surveillance and prevention programs.
|
|
| 3. |
- Bonassi, Stefano, et al.
(författare)
-
Chromosomal aberration frequency in lymphocytes predicts the risk of cancer: results from a pooled cohort study of 22 358 subjects in 11 countries
- 2008
-
Ingår i: Carcinogenesis. - : Oxford University Press (OUP). - 0143-3334 .- 1460-2180. ; 29:6, s. 1178-1183
-
Tidskriftsartikel (refereegranskat)abstract
- Mechanistic evidence linking chromosomal aberration (CA) to early stages of cancer has been recently supported by the results of epidemiological studies that associated CA frequency in peripheral lymphocytes of healthy individuals to future cancer incidence. To overcome the limitations of single studies and to evaluate the strength of this association, a pooled analysis was carried out. The pooled database included 11 national cohorts and a total of 22 358 cancer-free individuals who underwent genetic screening with CA for biomonitoring purposes during 1965-2002 and were followed up for cancer incidence and/or mortality for an average of 10.1 years; 368 cancer deaths and 675 incident cancer cases were observed. Subjects were classified within each laboratory according to tertiles of CA frequency. The relative risk (RR) of cancer was increased for subjects in the medium [RR = 1.31, 95% confidence interval (CI) = 1.07-1.60] and in the high (RR = 1.41; 95% CI = 1.16-1.72) tertiles when compared with the low tertile. This increase was mostly driven by chromosome-type aberrations. The presence of ring chromosomes increased the RR to 2.22 (95% CI = 1.34-3.68). The strongest association was found for stomach cancer [RRmedium = 1.17 (95% CI = 0.37-3.70), RRhigh = 3.13 (95% CI = 1.17-8.39)]. Exposure to carcinogens did not modify the effect of CA levels on overall cancer risk. These results reinforce the evidence of a link between CA frequency and cancer risk and provide novel information on the role of aberration subclass and cancer type.
|
|
| 4. |
|
|
| 5. |
- Latvala, Siiri, 1987-
(författare)
-
Development and comparison of in vitro toxicity methods for nanoparticles : Focus on lung cell exposure
- 2016
-
Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Concerns for the toxic effects of airborne nanoparticles have been raised along with the increasing production of nanostructured materials. However, the health risks of nanoparticle exposure are currently not fully understood. The most commonly used techniques to study nanoparticle toxicity, both in vivo and in vitro, have several limitations. These include for example challenges regarding dosimetry or the lack of similarity of overall exposure conditions and the physico-chemical particle characteristics. Therefore, there is a need for more advanced methods to study the pulmonary toxicity of airborne nanoparticles.This thesis presents the use of air-liquid interface (ALI) systems as a possible approach to this challenge. While utilizing the direct deposition of airborne nanoparticles on lung cell cultures, the ALI approach can more realistically mimic the characteristics of the human respiratory tract and the interactions of airborne particles with lung cells. This allows for a better understanding of the health risks posed by inhalation exposure to nanoparticles.Two different ALI systems were investigated and their use was compared to submerged exposure methods. One of the ALI exposure systems utilizes electrostatic force in order to make the deposition of charged airborne nanoparticles more efficient, while the other system operates by the diffusion of airborne nanoparticles. ALI and submerged exposure methods were used for investigating the cytotoxicity and genotoxicity of Ni-containing nanoparticles as well as the cytotoxicity and inflammatory potential of CeO2-nanoparticles. While Ag-nanoparticles were used as a test material during the development of the electrostatic ALI system, their cytotoxicity was investigated in ALI exposure. In conclusion, the ALI exposure methods provide more realistic conditions and make the particle dosimetry more controllable.
|
|
