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* Context.--Standards for pathology reporting of cancer are foundational to national and international benchmarking, epidemiology, and clinical trials, with international standards for pathology reporting of cancer being undertaken through the International Collaboration on Cancer Reporting (ICCR). Objective.--To develop standardized templates for brain tumor diagnostic pathology reporting. Design.--As a response to the 2016 updated 4th edition of the WHO (World Health Organization) Classification of Tumours of the Central Nervous System (2016 CNS WHO), an expert ICCR committee developed data sets to facilitate reporting of brain tumors that are classified histologically and molecularly by the 2016 CNS WHO; as such, this represents the first combined histologic and molecular ICCR data set, and required a novel approach with 3 highly related data sets that should be used in an integrated manner. Results.--The current article and accompanying ICCR Web site describe reporting data sets for central nervous system tumors in the hope that they provide easy-to-use and highly reproducible means to issue diagnostic reports in consort with the 2016 CNS WHO. Conclusions.--The consistent use of these templates will undoubtedly prove useful for patient care, clinical trials, epidemiologic studies, and monitoring of neuro-oncologic care around the world. (Arch Pathol Lab Med. 2020;144:196-206; doi: 10.5858/arpa.2018-0565-OA), The value of a structured or synoptic approach to cancer reporting, leading to improvement in the quality and completeness of pathology cancer reports, has been recognized through many studies (1-4) [...]

Background The serum biomarker cancer antigen 125 (CA125) is widely used as an investigation for possible ovarian cancer in symptomatic women presenting to primary care. However, its diagnostic performance in this setting is unknown. We evaluated the performance of CA125 in primary care for the detection of ovarian and non-ovarian cancers. Methods and findings We studied women in the United Kingdom Clinical Practice Research Datalink with a CA125 test performed between 1 May 2011-31 December 2014. Ovarian and non-ovarian cancers diagnosed in the year following CA125 testing were identified from the cancer registry. Women were categorized by age: A total of 50,780 women underwent CA125 testing; 456 (0.9%) were diagnosed with ovarian cancer and 1,321 (2.6%) with non-ovarian cancer. Of women with a CA125 level [greater than or equal to]35 U/ml, 3.4% aged Conclusions CA125 is a useful test for ovarian cancer detection in primary care, particularly in women [greater than or equal to]50 years old. Clinicians should also consider non-ovarian cancers in women with high CA125 levels, especially if ovarian cancer has been excluded, in order to prevent diagnostic delay. Our results enable clinicians and patients to determine the estimated probability of ovarian cancer and all cancers at any CA125 level and age, which can be used to guide individual decisions on the need for further investigation or referral., Author(s): Garth Funston 1,*, Willie Hamilton 2, Gary Abel 2, Emma J. Crosbie 3,4, Brian Rous 5, Fiona M. Walter 1 Introduction Ovarian cancer is the eighth most common cancer [...]

The detailed structural studies of lead that provide critical insights into the mechanism by which lead alters the activity of the proteins containing thoi-rich structural zinc-binding sites is reported. Lead binds in a three-coordinate mode and in a geometry that is fundamentally different from the natural coordination of zinc in these sites, which explains why lead disrupts the structure of zinc-binding peptides and thus provides the first detailed molecular understanding of the development toxicity of lead.

Metal-binding studies with DNA-binding domain of human estrogen receptor alpha and rat glucocorticoid receptor indicate that cobalt binds to both sites with similar affinities, while zinc binds to each of the two sites in the DNA-binding domains of steroid receptor. Data suggest there is hardly any interaction between the two metal sites in tems of metal binding.