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Thursday, September 27, 2012

Public Concern?

Controversial paper that revels link between "Genetically modified maize", toxicity and cancer published...




Available online 19 September 2012

Long term toxicity of a Roundup herbicide and a Roundup-tolerant genetically modified maize

  • a University of Caen, Institute of Biology, CRIIGEN and Risk Pole, MRSH-CNRS, EA 2608, Esplanade de la Paix, Caen Cedex 14032, France
  • b University of Verona, Department of Neurological, Neuropsychological, Morphological and Motor Sciences, Verona 37134, Italy
  • c University of Caen, UR ABTE, EA 4651, Bd Maréchal Juin, Caen Cedex 14032, France
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Abstract

The health effects of a Roundup-tolerant genetically modified maize (from 11% in the diet), cultivated with or without Roundup, and Roundup alone (from 0.1 ppb in water), were studied 2 years in rats. In females, all treated groups died 2–3 times more than controls, and more rapidly. This difference was visible in 3 male groups fed GMOs. All results were hormone and sex dependent, and the pathological profiles were comparable. Females developed large mammary tumors almost always more often than and before controls, the pituitary was the second most disabled organ; the sex hormonal balance was modified by GMO and Roundup treatments. In treated males, liver congestions and necrosis were 2.5–5.5 times higher. This pathology was confirmed by optic and transmission electron microscopy. Marked and severe kidney nephropathies were also generally 1.3–2.3 greater. Males presented 4 times more large palpable tumors than controls which occurred up to 600 days earlier. Biochemistry data confirmed very significant kidney chronic deficiencies; for all treatments and both sexes, 76% of the altered parameters were kidney related. These results can be explained by the non linear endocrine-disrupting effects of Roundup, but also by the overexpression of the transgene in the GMO and its metabolic consequences.

Highlights

► A Roundup-tolerant maize and Roundup provoked chronic hormone and sex dependent pathologies. ► Female mortality was 2–3 times increased mostly due to large mammary tumors and disabled pituitary. ► Males had liver congestions, necrosis, severe kidney nephropathies and large palpable tumors. ► This may be due to an endocrine disruption linked to Roundup and a new metabolism due to the transgene. ► GMOs and formulated pesticides must be evaluated by long term studies to measure toxic effects..

Abbreviations

  • GM, genetically modified; 
  • R, Roundup; 
  • MRL, maximal residual levels; 
  • GMO, genetically modified organism; 
  • OECD, Organization for Economic Co-operation and Development; 
  • GT, glutamyl-transferase; 
  • PCA, principal component analysis; 
  • PLS, partial least-squares; 
  • OPLS, orthogonal partial least-squares; 
  • NIPALS, Nonlinear Iterative Partial Least Squares; 
  • OPLS-DA, Orthogonal Partial Least Squares Discriminant Analysis; 
  • G, glycogen; 
  • L, lipid droplet; 
  • N, nucleus; 
  • R, rough endoplasmic reticulum (on microscopy pictures only); 
  • U, urinary; 
  • UEx, excreted in urine during 24 h; 
  • APPT, Activated Partial Thromboplastin Time; 
  • MCV, Mean Corpuscular Volume; 
  • PT, Prothrombine Time;
  • RBC, Red Blood Cells; 
  • ALT, alanine aminotransferase; 
  • MCHC, Mean Corpuscular Hemoglobin Concentration; 
  • A/G, Albumin/Globulin ratio; 
  • WBC, White Blood Cells; 
  • AST, aspartate aminotransferase

Keywords

  • GMO; 
  • Roundup; 
  • NK603; 
  • Rat; 
  • Glyphosate-based herbicides; 
  • Endocrine disrupting effects

Sunday, September 23, 2012

New Step in Breast Cancer Research


The Cancer Genome Atlas Network publish online new masterpiece paper


Comprehensive molecular portraits of human breast tumours

Nature
 
(2012)
 
doi:10.1038/nature11412
Received
 
Accepted
 
Published online
 

Abstract

We analysed primary breast cancers by genomic DNA copy number arrays, DNA methylation, exome sequencing, messenger RNA arrays, microRNA sequencing and reverse-phase protein arrays. Our ability to integrate information across platforms provided key insights into previously defined gene expression subtypes and demonstrated the existence of four main breast cancer classes when combining data from five platforms, each of which shows significant molecular heterogeneity. Somatic mutations in only three genes (TP53PIK3CA and GATA3) occurred at >10% incidence across all breast cancers; however, there were numerous subtype-associated and novel gene mutations including the enrichment of specific mutations inGATA3PIK3CA and MAP3K1 with the luminal A subtype. We identified two novel protein-expression-defined subgroups, possibly produced by stromal/microenvironmental elements, and integrated analyses identified specific signalling pathways dominant in each molecular subtype including a HER2/phosphorylated HER2/EGFR/phosphorylated EGFR signature within the HER2-enriched expression subtype. Comparison of basal-like breast tumours with high-grade serous ovarian tumours showed many molecular commonalities, indicating a related aetiology and similar therapeutic opportunities. The biological finding of the four main breast cancer subtypes caused by different subsets of genetic and epigenetic abnormalities raises the hypothesis that much of the clinically observable plasticity and heterogeneity occurs within, and not across, these major biological subtypes of breast cancer.

Monday, September 10, 2012

High Priority Areas for Evidence Generation








http://www.youtube.com/watch?v=4YluAIjeI2Q&hd=1

The Cancer Puzzle

Siddhartha Mukherjee's fascination with cancer is rooted not just in how to fight it, but in where it originated. Discovering almost nothing on the subject, the cancer physician and researcher wrote "Emperor of All Maladies: A Biography of Cancer," that explores the history of the disease that causes one quarter of all American deaths.