Bruce Ames

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Bruce Ames
Bruce Ames.jpg
Ames in 2003
Born
Bruce Nathan Ames

(1928-12-16) December 16, 1928 (age 95) [1]
NationalityAmerican
Alma mater California Institute of Technology,
Cornell University
Known for Ames test
SpouseGiovanna Ferro-Luzzi Ames
Awards Charles S. Mott Prize (1983)
Tyler Prize for Environmental Achievement (1985)
AIC Gold Medal (1981)
Japan Prize (1997)
National Medal of Science (1998)
Thomas Hunt Morgan Medal (2004)
Scientific career
Fields Molecular Biology, Biochemistry
Institutions University of California, Berkeley
Children's Hospital Oakland Research Institute
National Institutes of Health
Thesis The biosynthesis of histidine in Neurospora crassa  (1953)
Doctoral advisor Herschel K. Mitchell and Mary B. Mitchell

Bruce Nathan Ames (born December 16, 1928) is a prominent American biochemist. He is a professor of biochemistry and Molecular Biology Emeritus at the University of California, Berkeley, and was a senior scientist at Children's Hospital Oakland Research Institute (CHORI). [2] Throughout his career, Dr. Ames has made significant contributions to understanding the mechanisms of mutagenesis and DNA repair. One of his most notable achievements is the invention of the Ames test, a widely used assay for easily and cheaply evaluating the mutagenicity of compounds. [3] The test revolutionized the field of toxicology and has played a crucial role in identifying numerous environmental and industrial carcinogens.

Contents

Biography

Ames, raised in New York City, is a graduate of the Bronx High School of Science. His undergraduate studies were at Cornell University in Ithaca, New York, and his graduate studies were completed at the California Institute of Technology. [4]

Ames was elected a Fellow of the American Academy of Arts and Sciences in 1970. [5]

He is a recipient of the Bolton S. Corson Medal in 1980, Tyler Prize for Environmental Achievement in 1985, the Japan Prize in 1997, the National Medal of Science in 1998 and the Thomas Hunt Morgan Medal in 2004, [6] among many others.

His research focuses on cancer and aging and he has authored over 550 scientific publications. He is among the few hundred most-cited scientists in all fields. [7]

Ames' most recent research included identifying agents that delay the mitochondrial decay of aging, understanding the role of mitochondrial decay in aging, particularly in the brain, optimizing micronutrient intakes in the population to prevent disease, malnutrition, and obesity. He is also interested in mutagens as they relate to cancer prevention and aging. [8]

Dr. Ames received more than $650,000 in support from the National Foundation for Cancer Research between 1998 and 2007. [9]

He is married to Dr. Giovanna Ferro-Luzzi Ames, who was also a professor of biochemistry at the University of California, Berkeley.

Ames on synthetic carcinogens

In the 1970s, Bruce Ames developed the Ames test which is a cheap and convenient assay for mutagens and therefore potential carcinogens. Previous carcinogenic testing used live animals, and the procedures are expensive and time-consuming. This made animal testing impractical for use in screening on a wide scale, and reduced the number of compounds that could be tested. The Ames test on the other hand uses the bacteria Salmonella typhimurium to test for mutagens, and is considerably cheaper and faster. The Ames test became widely used as an initial screen for possible carcinogens and has been used to identify potential carcinogens previously used in commercial products. [10] Their identification led to some of those formulations, such as chemicals used in hair dye, [11] being withdrawn from commercial use. The ease with which Ames test allows widely used chemicals to be identified as possible carcinogens made him an early hero of environmentalism. [3]

Subsequent work in Ames' lab involved looking at an overview of what was mutagenic or carcinogenic, and to what degree. Previously, scientists tended to only look for positive or negative results without considering the magnitude of the effect, which meant that as more and more items were shown to be potentially mutagenic, there was no system for evaluating the relative dangers. He also continued to test various natural and man-made compounds, and discovered that, despite what he and others had assumed, naturally occurring compounds were not turning out to be benign as compared to man-made ones. His continued work eventually led to his falling out of favor with many environmentalists. As natural chemicals turned out to also be frequently mutagenic, he argued that environmental exposure to manufactured chemicals may be of limited relevance to human cancer, even when such chemicals are mutagenic in an Ames test and carcinogenic in rodent assays. [12] He contended that most human genetic damage arises from essential micronutrients lacking in poor diets and the oxidation of DNA during normal metabolism, and that the most important environmental carcinogens may include some whose chief effect is to cause the chronic division of stem cells whereby the normal protective mechanisms of a cell become less effective.

He argued against the banning of synthetic pesticides and other chemicals such as Alar which have been shown to be carcinogenic. Ames published results showing that many ordinary food products would be found carcinogenic according to the same criteria. [3] [13] Ames was concerned that overzealous attention to the relatively minor health effects of trace quantities of carcinogens may divert scarce financial resources away from major health risks, and cause public confusion about the relative importance of different hazards. Ames considered himself a leading “contrarian in the hysteria over tiny traces of chemicals that may or may not cause cancer", and said that "if you have thousands of hypothetical risks that you are supposed to pay attention to, that completely drives out the major risks you should be aware of." [14]

Notable awards

Related Research Articles

<span class="mw-page-title-main">Ames test</span> Biological testing method

The Ames test is a widely employed method that uses bacteria to test whether a given chemical can cause mutations in the DNA of the test organism. More formally, it is a biological assay to assess the mutagenic potential of chemical compounds. A positive test indicates that the chemical is mutagenic and therefore may act as a carcinogen, because cancer is often linked to mutation. The test serves as a quick and convenient assay to estimate the carcinogenic potential of a compound because standard carcinogen assays on mice and rats are time-consuming and expensive. However, false-positives and false-negatives are known.

Mutagenesis is a process by which the genetic information of an organism is changed by the production of a mutation. It may occur spontaneously in nature, or as a result of exposure to mutagens. It can also be achieved experimentally using laboratory procedures. A mutagen is a mutation-causing agent, be it chemical or physical, which results in an increased rate of mutations in an organism's genetic code. In nature mutagenesis can lead to cancer and various heritable diseases, and it is also a driving force of evolution. Mutagenesis as a science was developed based on work done by Hermann Muller, Charlotte Auerbach and J. M. Robson in the first half of the 20th century.

<span class="mw-page-title-main">Mutagen</span> Physical or chemical agent that increases the rate of genetic mutation

In genetics, a mutagen is a physical or chemical agent that permanently changes genetic material, usually DNA, in an organism and thus increases the frequency of mutations above the natural background level. As many mutations can cause cancer in animals, such mutagens can therefore be carcinogens, although not all necessarily are. All mutagens have characteristic mutational signatures with some chemicals becoming mutagenic through cellular processes.

Genotoxicity is the property of chemical agents that damage the genetic information within a cell causing mutations, which may lead to cancer. While genotoxicity is often confused with mutagenicity, all mutagens are genotoxic, but some genotoxic substances are not mutagenic. The alteration can have direct or indirect effects on the DNA: the induction of mutations, mistimed event activation, and direct DNA damage leading to mutations. The permanent, heritable changes can affect either somatic cells of the organism or germ cells to be passed on to future generations. Cells prevent expression of the genotoxic mutation by either DNA repair or apoptosis; however, the damage may not always be fixed leading to mutagenesis.

<span class="mw-page-title-main">Auxotrophy</span> Inability to synthesize an organic compound required for growth

Auxotrophy is the inability of an organism to synthesize a particular organic compound required for its growth. An auxotroph is an organism that displays this characteristic; auxotrophic is the corresponding adjective. Auxotrophy is the opposite of prototrophy, which is characterized by the ability to synthesize all the compounds needed for growth.

<span class="mw-page-title-main">Methylcholanthrene</span> Chemical compound

Methylcholanthrene is a highly carcinogenic polycyclic aromatic hydrocarbon produced by burning organic compounds at very high temperatures. Methylcholanthrene is also known as 3-methylcholanthrene, 20-methylcholanthrene or the IUPAC name 3-methyl-1,2-dyhydrobenzo[j]aceanthrylene. The short notation often used is 3-MC or MCA. This compound forms pale yellow solid crystals when crystallized from benzene and ether. It has a melting point around 180 °C and its boiling point is around 280 °C at a pressure of 80 mmHg. Methylcholanthrene is used in laboratory studies of chemical carcinogenesis. It is an alkylated derivative of benz[a]anthracene and has a similar UV spectrum. The most common isomer is 3-methylcholanthrene, although the methyl group can occur in other places.

<span class="mw-page-title-main">Methyl carbamate</span> Chemical compound

Methyl carbamate (also called methylurethane, or urethylane) is an organic compound and the simplest ester of carbamic acid (H2NCO2H). It is a colourless solid.

Benzo(<i>j</i>)fluoranthene Chemical compound

Benzo[j]fluoranthene (BjF) is an organic compound with the chemical formula C20H12. Classified as a polycyclic aromatic hydrocarbon (PAH), it is a colourless solid that is poorly soluble in most solvents. Impure samples can appear off white. Closely related isomeric compounds include benzo[a]fluoranthene (BaF), bendo[b]fluoranthene (BbF), benzo[e]fluoranthene (BeF), and benzo[k]fluoranthene (BkF). BjF is present in fossil fuels and is released during incomplete combustion of organic matter. It has been traced in the smoke of cigarettes, exhaust from gasoline engines, emissions from the combustion of various types of coal and emissions from oil heating, as well as an impurity in some oils such as soybean oil.

The Environmental Mutagenesis and Genomics Society (EMGS) is a scientific society "for the promotion of critical scientific knowledge and research into the causes and consequences of damage to the genome and epigenome in order to inform and support national and international efforts to ensure a healthy, sustainable environment for future generations."

Wang Aiping is a Chinese pharmacologist and toxicologist. For over 20 years, Wang has researched drug and toxicity testing and has experience in new drug development. Since 2001, he has been Director of Drug Safety Evaluation and Research at the Academy of Medical Sciences, Peking Union Medical College and was also made General Manager of Technological development at Peking Union Medical College's Jianhao Pharmaceutical Technology Development Co., Ltd.

For pharmacology and genetics, the Umu Chromotest, first developed and published by Oda et al., is a biological assay (bioassay) to assess the genotoxic potential of chemical compounds. It is based on the ability of DNA-damaging agents to induce the expression of the umu operon. In connection with the damage inducible (din) genes recA, lexA and umuD, the umuC gene is essentially involved in bacterial mutagenesis through the SOS response.

<span class="mw-page-title-main">Takashi Sugimura</span> Japanese cancer researcher (1926–2020)

Takashi Sugimura was a Japanese biochemist, famous for research on chemical carcinogens. He received the Japan Prize for the contribution to establishment of fundamental concept on causes of cancer. He was elected as President of the Japan Academy on October 15, 2013, serving till 2016 and was replaced with Hiroshi Shiono.

Rajani A. Bhisey is an Indian scientist. She specializes in the field of environmental carcinogenesis and molecular epidemiology of cancer, occupational hazards.

Bernd Kaina, born on 7 January 1950 in Drewitz, is a German biologist and toxicologist. His research is devoted to DNA damage and repair, DNA damage response, genotoxic signaling and cell death induced by carcinogenic DNA damaging insults.

<span class="mw-page-title-main">Francesco De Lorenzo</span> Italian politician

Francesco De Lorenzo is an Italian physician and politician and is a member of the Italian Liberal Party.

<span class="mw-page-title-main">Curtis C. Harris</span> American cancer researcher

Curtis. C. Harris is the head of the Molecular Genetics and Carcinogenesis Section and chief of the Laboratory of Human Carcinogenesis at the Center for Cancer Research of the National Cancer Institute, NIH.

Gareth Jenkins is a professor of molecular carcinogenesis at Swansea University Medical School. Based in the Institute of Life Science, his interests include the study of DNA mutation induction and the role of DNA mutations as diagnostic biomarkers for cancer. He is also director of research of the medical school and a “research leader” for Health and Care Research Wales. Jenkins' research gained much recognition during 2016 when his revolutionary cancer-detecting blood test was widely covered in the British press.

<span class="mw-page-title-main">Bioassay</span> Analytical method to determine potency and effect of a substance

A bioassay is an analytical method to determine the potency or effect of a substance by its effect on living animals or plants, or on living cells or tissues. A bioassay can be either quantal or quantitative, direct or indirect. If the measured response is binary, the assay is quantal; if not, it is quantitative.

Sheldon Wolff was an American radiobiologist, cytogeneticist, and environmental health expert on mutagenic chemicals.

<span class="mw-page-title-main">Bruce Hammock</span> American entomologist and toxicologist

Dr. Bruce Hammock is an American entomologist, chemist and toxicologist. He is known for his research regarding improving pest control agents, monitoring and determining the human and environmental health effects of pesticides and in medicine work on the inflammation resolving branch of the arachidonate cascade leading to a drug candidate to treat pain and inflammatory disease. Additionally, he made many advances in U.S. agriculture which led to him receiving the Frasch and Spencer Awards of the ACS and the Alexander von Humboldt Award in Agriculture. His early work tested the basic hypothesis in both insects and mammals that regulation of chemical mediators could be as much by specific degradation as by biosynthesis. He exploited this fundamental knowledge both in agriculture and in human pharmacology.

References

  1. Dr. Bruce N. Ames. japanprize.jp
  2. "Biography and information". CHORI. Archived from the original on 2017-12-13. Retrieved 2008-09-13.
  3. 1 2 3 Synthetic v. Natural Pesticides. New York Times (June 6, 2007)
  4. Ames BN (February 2003). "An enthusiasm for metabolism". J. Biol. Chem. 278 (7): 4369–80. doi: 10.1074/jbc.X200010200 . PMID   12496254.
  5. "Book of Members, 1780–2010: Chapter A" (PDF). American Academy of Arts and Sciences. Retrieved 17 April 2011.
  6. Smith, Gerald R; Johnston Mark (February 2004). "The 2004 Thomas Hunt Morgan Medal". Genetics . 166 (2): 645–6. doi:10.1534/genetics.166.2.645. ISSN   0016-6731. PMC   1470756 . PMID   15020453.
  7. "About Dr. Ames". Bruce Ames official website.
  8. Bruce N. Ames. University of California
  9. Salisbury, Franklin (2001). "National Foundation for Cancer Research". Neoplasia. 3 (1): 88–90. doi:10.1038/sj.neo.7900130. PMC   1505022 .
  10. Ames, B. N. (1979). "Identifying environmental chemicals causing mutations and cancer" (PDF). Science . 204 (4393): 587–593. Bibcode:1979Sci...204..587A. doi:10.1126/science.373122. JSTOR   1748159. PMID   373122.
  11. Ames, Bruce; Kammen H.O. (June 1975). "Hair Dyes Are Mutagenic: Identification of a Variety of Mutagenic Ingredients". Proceedings of the National Academy of Sciences. 72 (6): 2423–2427. Bibcode:1975PNAS...72.2423A. doi: 10.1073/pnas.72.6.2423 . PMC   432771 . PMID   1094469.
  12. Forman, D. (1991). "Ames, the Ames test, and the causes of cancer". BMJ (Clinical Research Ed.). 303 (6800): 428–429. doi:10.1136/bmj.303.6800.428. PMC   1670593 . PMID   1912830.
  13. Gold, L.S., Slone, T.H., Ames, B.N., and Manley, N.B., Pesticide Residues in Food and Cancer Risk: A Critical Analysis. In: Handbook of Pesticide Toxicology, Second Edition (R. Krieger, ed.), San Diego, CA: Academic Press, pp. 799-843 (2001)
  14. Twombly, R. (2001). "Federal carcinogen report debuts new list of nominees". Journal of the National Cancer Institute. 93 (18): 1372. doi: 10.1093/jnci/93.18.1372 . PMID   11562386.