Tuesday, 28 October 2008

Mesothelioma Diesease And Asbestos Induced Scarring Information

One interesting study is called, “Radiological abnormalities and asbestos exposure among custodians of the New York City Board of Education” by Levin, S.M. ; Selikoff, I.J. - Annals of the New York Academy of Sciences; (United States); Journal Volume: 643. Here is an excerpt: “Six hundred sixty custodians employed by the New York City Board of Education underwent examination from 1985 through 1987 for asbestos-related disease and other general medical conditions by the clinical staff of the Division of Environmental and Occupational Medicine of the Mount Sinai School of Medicine of the City University of New York. Two-thirds of the men (no women were examined) were 20 or more years from onset of any custodial work, with 44% having had at least 20 years of employment as custodial workers in New York City Board of Education schools. Twenty-four percent had begun custodial work in buildings 30 or more years earlier. Findings among them were of particular interest since asbestos-related disease might forecast what might be expected among school custodians with less seniority. Since the Board of Education, in selecting custodians for examination, had chosen only custodians currently employed, the study group comprised men still working in the school system. These, then, represented a survivor population'. Although a considerable amount of clinical information was obtained, abnormalities on chest X-ray consistent with asbestos-induced scarring were used as the key index of disease resulting from exposure to asbestos. Since scarring of the lung tissue may be present but undetectable on standard chest radiographs (a relatively insensitive diagnostic technique), the prevalence of abnormality on X-ray film represents a conservative estimate of the actual burden of scarring lung disease in the group. Such changes are indicative of previous asbestos exposure, however, and provide evidence of an increased risk of later asbestos-related malignancy. Overall, abnormalities on chest X-ray consistent with asbestos-related scarring were found in 28% of the men examined.”

Another study is called, “Magnetic lung measurements in relation to occupational exposure in asbestos miners and millers of Quebec” - Environmental Research Volume 26, Issue 2, December 1981, Pages 535-550 by David Cohen, Thomas S. Crowther1Graham W. Gibbs2 and Margaret R. Becklake. Here is an excerpt: “Abstract - Fe3O4 particles (ferrimagnetic) are usually attached to asbestos fibers (nonferrimagnetic) in the chrysotile asbestos mining and milling industries; therefore, a magnetic measurement of Fe3O4 in the lungs of workers in these industries could help determine the amount of asbestos which has been inhaled and retained in their lungs. As a first assessment of this method, magnetic measurements were made of Fe3O4 in the lungs of 115 miners and millers in Quebec. These measurements at an industrial site were found to be feasible and practical; however, the amount of Fe3O4 seen in the lungs of those with welding exposure was large enough to mask the Fe3O4 contributed by asbestos, and this subgroup was considered separately. For the remainder (nonwelders), the amount of Fe3O4 was plotted against a total dust exposure index (asbestos and other dust) estimated for each worker. Although the correlation between these quantities was not high, it was statistically significant at the 1% level. Because retained asbestos is likely to increase with increasing exposure to total dust, this correlation suggests that a magnetic lung measurement of a chrysotile miner or a miller does reflect, to some extent, the amount of asbestos in his lung. There was considerable scatter in the data, partly due to individual variations in deposition and clearance, to which this method is sensitive. When the data of only the nonsmokers were plotted, the amount of Fe3O4 was greater than for the total group of nonwelders. This is consistent with previous findings that less dust is deeply deposited in the lungs of smokers, due to constriction of small airways.”

Another study is called, “The histopathology and ultrastructure of pleural mesotheliomas produced in the rat by injections of crocidolite asbestos.” By Davis JM. - Br J Exp Pathol. 1979 Dec;60(6):642-52. Here is an excerpt: “Abstract - Primary tumours of the pleural cavity were produced in rats by the intrapleural injection of crocidolite asbestos. Their histological structure as seen with both light and electron microscopy was very variable and tumours frequently contained elements of both connective-tissue and epithelial type. In some instances the connective-tissue elements predominated from the start and the earliest tumour nodules consisted mainly of pleomorphic connective-tissue cells with only a few layers of cells more nearly epithelial in type on the surface. This pattern was largely retained when tumour nodules increased in size and coalesced, but in the deeper layers of advanced tumours the pleomorphic connective-tissue pattern was often replaced by a more uniform spindle-cell form. Other tumours were more predominantly epithelial in type, showing either a papillary pattern with rounded epithelial cells growing in solid columns, or a vesicular form in which large tissue spaces, often intracellular, were lined by very thin layers of extended cell cytoplasm. Whereas early tumours showed only one histological pattern, the more advanced stages often exhibited areas of all 3, so that there seemed to be some degree of histological mutability. The spindle-cell areas of advanced tumours frequently showed evidence of direct invasion of the surrounding tissue but this was never seen with the epithelial forms of rat mesothelioma.”

If you found any of these excerpts interesting, please read the studies in their entirety. We all owe a debt of gratitude to these fine researchers.

Thursday, 23 October 2008

Growth Factors And Cognate Receptors For Mesothelioma Information

One interesting study is called, “Characterization of Platelet-derived Growth Factor and Platelet-derived Growth Factor Receptor Expression in Asbestos-induced Rat Mesothelioma” - Cancer Res January 15, 1992 52; 301 by Cheryl Walker, Edilberto Bermudez, Wendy Stewart, James Bonner, Christopher J. Molloy, and Jeffrey Everitt. Here is an excerpt: “Abstract - Although altered expression of platelet-derived growth factor (PDGF) is a hallmark of human mesothelioma, expression of PDGF receptors has not been characterized in this cell type. In addition, the expression of this growth factor and its cognate receptor in rodent mesothelioma has not been investigated. In this study, examination of transformed mesothelial cells derived from asbestos-induced rat mesotheliomas revealed that these cells expressed high affinity PDGF receptors (Kd = 0.5 nm) and receptor number was 1.6 × 105/cell. Western analysis using antibodies specific for either the ±-type or ²-type PDGF receptor and Northern analysis using probes specific for ±- and ²-type receptor RNA transcripts indicated that these cells expressed ²-type PDGF receptors but that ±-type receptors could not be detected. However, when the mesothelioma-derived cells were examined for the expression of PDGF, no expression of this growth factor could be detected. The transformed cells expressed no detectable A- or B-chain PDGF RNA transcripts; and using a competitive enzyme immunoassay specific for isoforms containing the B chain of PDGF and a sandwich enzyme-linked immunosorbent assay specific for A-chain-containing isoforms, neither AA, nor AB, nor BB isoforms of this growth factor could be detected in medium conditioned by these cells. The absence of alterations in PDGF expression in rat mesothelioma, in contrast to the data for the human disease, suggests that the production of this growth factor by transformed mesothelial cells may be species specific.”

Another interesting study is called, “Leaching of Constituents of Chrysotile Asbestos in vivo” - Nature 215, 441 - 442 (22 July 1967); by A. Holmes & A. Morgan - Health Physics and Medical Division, Atomic Energy Research Establishment, Harwell, Didcot, Berkshire. Here is an excerpt: “IN recent years, Wagner1 and Selikoff et al. 2 have shown that a rare tumour, the diffuse mesothelioma of the pleura and peritoneum, is associated with past exposure to asbestos. It appears that the amount of asbestos required to produce these tumours is small and that the latent period is very long. The connexion between exposure to asbestos and the production of mesotheliomas is being studied in a number of laboratories, and the possibility that trace metal constituents or contaminating oils may have a role has been suggested3. As yet, little is known about the fate of inhaled asbestos fibres and in particular about their movement out of the lung into other organs. The experiment described here was planned to assess the possibility of using radioactivity, induced in asbestos fibres by neutron irradiation, to trace their translocation in rats after administration by intrapleural injection.”

Another study is called, “Ferruginous bodies in sputa of former asbestos workers.” By Farley ML, Greenberg SD, Shuford EH Jr, Hurst GA, Spivey CG, Christianson CS - Acta Cytol. 1977 Sep-Oct; 21(5):693-700. Here is an excerpt: “Abstract - Routine cytopathologic examinations were performed at six-month intervals on sputum specimens from 628 former asbestos workers and 138 control patients. The occurrence of ferruginous bodies in sputa is found to increase as a logarithmic function of the length of occupational exposure to asbestos in workdays. No significant association is found between the occurrence of ferruginous bodies and the worker's age, smoking history, degree of cellular epithelial atypia, or time since last exposure. We conclude that the presence of ferruginous bodies in sputa is evidence of probable significant occupational exposure to asbestos dust. Their absence does not indicate lack of exposure. We can also conclude that routine cytopathology procedures are sufficient for the detection of ferruginous bodies in sputa.”

If you found any of these excerpts interesting, please read the studies in their entirety. We all owe a debt of gratitude to these fine researchers.

Thursday, 16 October 2008

Possible Causes Of Mesothelioma Information and Article

The five main causes attributed towards the cancer called Mesothelioma are: asbestos exposure, radiation, simian virus, tobacco use, and zeolite.

What is asbestos? It's a naturally-occurring fibrous mineral known for its durability, fire resistance, and insulating properties, was used in thousands of products in the 20th century, including construction materials, machinery, automobiles, and consumer goods. Use of asbestos was banned in the early 1980s; however many companies made and sold this product right up until the ban. Malignant Mesothelioma has been validated by the scientific community to have one cause above all other causes: asbestos.

Radiation, like ionizing radiation, which consists of energetic forms of light, X-rays, and gamma rays are all used in the diagnosis of disease. However, a recent study has shown that such radiation can trigger mesothelioma in some people.

What is the Simian Virus? The abbreviation for Simian Virus is SV40. It's a polymavirus that is a DNA virus that can cause tumors, but often persists as a latent infection. The query is can a virus, like SV40 cause the cancer mesothelioma? According to a study done by the Cancer Research Center of the University of Hawaii found that SV40 is present in some people with malignant mesothelioma. During this study they injected SV40 virus into laboratory hamsters, 60 percent of which developed the disease and died of mesothelioma. Though scientists are not able to state that SV40 directly causes mesothelioma, they are willing to say that it may trigger cancer in people whose immune system are week.

It's a recognized proven fact that extended tobacco use could cause cancer. However, can it cause mesothelioma? Starting in 1952, the P. Lorillard Tobacco Company sold filter cigarettes under the Kent brand. These filters contained micronite which has 10mg of asbestos in each filter. Five years later, the group dumped the use of micronite filters; however, the contact with asbestos had already done irreparable damage to those exposed to asbestos. Asbestos has also been used in other widely-sold tobacco products through the years as well, including rolling papers and in pipe tobaccos, creating a link between the usage of tobacco and mesothelioma.

Zeolites are a category of naturally occurring crystalline mineral substances composed primarily of aluminum and silicon which can also be produced artificially. This substance isn't toxic in nature; however, it can form tiny fiber like structures similar to asbestos. Due to this truth, it's lead some medical researchers to conclude that there is a link between zeolites and mesothelioma. Zeolites are used in a wide variety of industries in the United States, especially the petroleum, plastics, and chemical industries and associated fields. Zeolite miners and processors are also regularly exposed to the substance.

Though these are five possible causes of mesothelioma, it is still possible to get mesothelioma without being exposed to these causes. However, if you have mesothelioma and suspect your contact with any of the five causes discussed it is important to contact a mesothelioma attorney. Mesothelioma lawyers can help you identify whether legal action is warranted and whether you might be entitled to financial compensation.

Wednesday, 8 October 2008

Mesothelioma And Pulmonary Decortication Information

Another interesting study is called, “Pleurectomy for mesothelioma.” By Brancatisano RP, Joseph MG, McCaughan BC - Department of Surgery, Repatriation General Hospital Concord, NSW. Med J Aust. 1991 Apr 1;154(7):455-7, 460. Here is an excerpt: “Abstract - OBJECTIVE: To assess the effectiveness and safety of parietal pleurectomy in establishing a tissue diagnosis and controlling pleural fluid accumulation in patients with pleural mesothelioma, and to assess the success of this procedure in effecting palliation. DESIGN AND SETTING: Fifty consecutive patients with pleural mesothelioma who underwent thoracotomy at the cardiothoracic units at Concord and Royal Prince Alfred Hospital were reviewed retrospectively. The male:female ratio was 4:1 and the mean age was 63 years. In only 11 of the 50 patients was a tissue diagnosis of mesothelioma made before surgery. INTERVENTIONS: At thoracotomy, subtotal parietal pleurectomy was performed in 45 of the 50 patients. In two patients biopsy alone was performed and three patients were treated by a chemical pleurodesis only, as pleurectomy was not technically possible. Pulmonary decortication was required in 28 patients to allow full expansion of the underlying lung for effective pleurodesis.

RESULTS: There was one postoperative death. The morbidity rate was 16%. Excluding the patient who died in the postoperative period, the median survival was 16 months, and ranged from three to 54 months, with 21% of patients surviving for more than two years. Only one patient developed a reaccumulation of pleural fluid.

CONCLUSIONS: Pleurectomy, with decortication when required, provides both a tissue diagnosis and effective control of pleural fluid accumulation and therefore excellent palliation in patients with pleural mesothelioma. We advocate early thoracotomy in these patients.”

Another interesting study is called, “Use of a “Replication-Restricted” Herpes Virus to Treat Experimental Human Malignant Mesothelioma” by John C. Kucharczuk1, Bruce Randazzo1, Michael Y. Chang, Kunjlata M. Amin, Ashraf A. Elshami, Daniel H. Sterman, Nabil P. Rizk, Katherine L. Molnar-Kimber, S. Moira Brown, Alasdair R. MacLean, Leslie A. Litzky, Nigel W. Fraser, Steven M. Albelda, and Larry R. Kaiser – Cancer Res February 1, 1997 57; 466 - Here is an excerpt: “Abstract - Modified, nonneurovirulent herpes simplex viruses (HSVs) have shown promise in the treatment of brain tumors. However, HSV-1 can infect and lyse a wide range of cell types. In this report, we show that HSV-1716, a mutant lacking both copies of the gene coding ICP-34.5, can effectively treat a localized i.p. malignancy. Human malignant mesothelioma cells supported the growth of HSV-1716 and were efficiently lysed in vitro. i.p. injection of HSV-1716 into animals with established tumor nodules reduced tumor burden and significantly prolonged survival in an animal model of non-central nervous system-localized human malignancy without dissemination or persistence after i.p. injection into SCID mice bearing human tumors.  These findings suggest that this virus may be efficacious and safe for use in localized human malignancies of nonneuronal origin such as malignant mesothelioma.

An interesting study is called, “Interleukin 6 and its relationship to clinical parameters in patients with malignant pleural mesothelioma.” By T. Nakano, A. P. Chahinian, M. Shinjo, A. Tonomura, M. Miyake, N. Togawa, K. Ninomiya, and K. Higashino - Br J Cancer. 1998 March; 77(6): 907–912. Here is an excerpt: “Abstract - The relationship between interleukin 6 (IL-6) levels and clinical parameters was studied in 25 patients with malignant pleural mesothelioma. The serum levels of IL-6, C-reactive protein, alpha1-acid glycoprotein and fibrinogen were significantly higher in mesothelioma than in lung adenocarcinoma with cytology-positive pleural effusion. Serum IL-6 levels correlated with the levels of the acute-phase proteins. We demonstrated a high incidence of thrombocytosis (48%) and a significant correlation between platelet count and the serum IL-6 level. The level of IL-6 in the pleural fluid of patients with mesothelioma was significantly higher than in the pleural fluid of patients with adenocarcinoma, and was about 60-1400 times higher than in the serum. However, even higher levels of IL-6 in the pleural fluid and of thrombocytosis were found in patients with tuberculous pleurisy. These results indicate that large amounts of IL-6 from the pleural fluid of patients with mesothelioma leak into the systemic circulation and induce clinical inflammatory reactions. These profiles are not specific to mesothelioma as similar profiles are found in patients with tuberculous pleurisy. However, the detection of a markedly increased level of IL-6 in pleural fluid argues against a diagnosis of adenocarcinoma.”


We all owe a debt of gratitude to these fine researchers for their work. If you found any of these excerpts helpful, please read the studies in their entirety.

Friday, 3 October 2008

Mesothelioma Lawyers Southern California Information

If you are looking for information about Mesothelioma Lawyers Southern California, you have come to the right place. But first, who are these people and what can they do for you?

Mesothelioma Lawyers are legal practitioners with the sole aim of assisting you claim your compensation when you diagnosed of Mesothelioma; a disease caused as a result of extreme exposure to asbestos. If you have been working in a manufacturing company, asbestos is a common term.

These lawyers do a very wonderful job by making sure you don’t suffer the disease. They believe you should be compensated; after all you got the disease as a result of your working with the said company. There have been successful stories where people have been able to claim millions of dollars in compensation from the company.

If you know someone who has been diagnosed of Mesothelioma, you can help out. There is Mesothelioma Lawyers Southern California who can help you out. They can help you file a lawsuit against the company and at the end of the day; you will be able to claim what rightly belongs to you.


The United States Laws purely supports Filing a lawsuit in order to claim your compensation provided you have this disease. It does not matter how severe your may be, the fact still remains that you have the disease and should be compensated. There are several professional Mesothelioma Lawyers Southern California who can help you out, when making your selection, go for those whose profession is based around industrial lawsuit so you can relax with the mindset of a victor.