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The CANCER RISK of BENZO[α] PYRENE Abstract # 30 Presented by My Linh Tran Math and Science Division San Jose City College Spring 2006 Instructor Dr. Adamczeski,Madeline.

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Presentation on theme: "The CANCER RISK of BENZO[α] PYRENE Abstract # 30 Presented by My Linh Tran Math and Science Division San Jose City College Spring 2006 Instructor Dr. Adamczeski,Madeline."— Presentation transcript:

1 The CANCER RISK of BENZO[α] PYRENE Abstract # 30 Presented by My Linh Tran Math and Science Division San Jose City College Spring 2006 Instructor Dr. Adamczeski,Madeline

2 ABSTRACT When people eat burnt barbequed food, they may carelessly consume significant amounts of carcinogens, some of which called aromatic hydrocarbons. The definition of aromatic hydrocarbon can be extended from simple one ring to substances that have two or more benzene-like rings joined together by common bonds (e.g. polycyclic aromatic hydrocarbons). Benzopyrene (BaP) is categorized as a polycyclic aromatic hydrocarbon and is recognized as one of the most carcinogenic of the group. BaP is formed from a reaction between one of the twenty essential amino acids and creatine in the process of cooking meats at high temperature. Creatine is an amino acid that does not occur in protein but is found in the muscle tissues of vertebrates both in the free form and as phosphocreatine (e.g. it supplies energy for muscle contraction). After eating BaP, our body attempts to rid of the foreign substance by converting it into a water-soluble compound for metabolism, a diol expoxide. This compound, in turn, reacts with and binds to cellular DNA. Consequently, diol expoxide alters DNA and mutates genes. This presentation introduces BaP, shows reaction mechanism involving BaP, and explains how BaP can cause cancer.

3 Benzopyrene- Polycyclic Aromatic Hydrocarbons and Mutations Seminar Outline Introduction: What is Benzopyrene? Burnt barbeque, meat, fish, How is it made? Where can we find it Structure C20H12 Toxicity data research Epoxidation Chemical evaluation Properties: Benzene Flat, sp2, conjugated pi electrons Stable Reacts with oxygen and other electrophiles Biological evaluation Metabolism: Liver MFO enzyme Water-soluble epoxy groups Reactions with epoxy groups Epoxides of benzopyrene DNA mutation It becomes similar to dA and dG General information Dose Duration Pathway Individual VI. Conclusion The dose makes the poison BBQ at low temperature Use thinner slice of meat Teriyaki sauce or turmeric-garlic sauce before barbeque

4 SUMMER BARBEQUE WOULD YOU EAT THIS? The well known Polycyclic Aromatic Hydrocarbon

5 OVERVIEW Introduction What is Benzo[α]pyrene? Chemical properties What is its effect on humans? How is it made? Where can we find it? Prevention

6 BENZO[α]PERENE (BaP) Yellow crystals or Powder Molecular formula: C20H12 Formula weight: 252.31 amu CAS No: 50-32-8 Boiling point: 495 o C Melting point: 176 oC RAT LD50 50mg / kg MOUSE LDLO 500mg / kg FROG LDLO 11 mg/kg

7 BARBEQUE and POLYCYCLIC and CANCER SOURCE: BURNT Barbeque EFFECT: Formed from a reaction between amino acids and creatine when meats are cooked at high temperature Creatine: an amino acid that does not occur in proteins but is found in the muscle tissue of vertebrates both in the free form and as phosphocreatine; supplies energy for muscle contraction CONSEQUENCE: MUTATION

8 · After eating or inhaling, body attempts to rid itself of the foreign substance by converting it into a water-soluble metabolism: DIOL EXPOXIDE DIOL EXPOXIDE Metabolite reacts with & binds to cellular DNA DIOL EXPOXIDE altering the DNA & leading to mutations or cancers HOW BaP CAUSE MUTATIONS?

9 STABILITY OF BaP Stable, incompatible with strong oxidizing agents Causes oxidation, gain one or more electrons, undergoes reduction, oxidation number of atom decrease

10 PERCHLORATES PEROXIDES PERMANGANATES CHLORATES NITRATES CHLORINE BROMINE FLOURINE

11 BaP- SITE of EPOXIDATION

12 http://www.nyu.edu/projects/geacintov/images/WE B_Figures/WEB_PAH2.jpg

13 SIMILAR to the BASES THEY REPLACE

14

15 HYDROLYSIS of EPOXIDE

16 (R,S,S,R) enantiomer: On reaction with DNA, DE derived (BaP) are largely selective for G adduct formation DIOL EPOXIDE HYDROLASE

17

18 DIOL EPOXIDE

19

20 DNA- DIOL EPOXIDE

21 Altered DNA by replication Altered RNA by transcription Incorrect protein synthesis Shortened DNA by replication through blockage Shortened RNA by transcription blockage

22 HOW ARE WE EXPOSED TO BaP? Breathing air contaminated by smoke from incomplete combustion & vehicle exhaust Eating meats and fish that have been smokes or charbroiled Smoking tobacco products

23 WHERE BaP CAN BE FOUND? Wildfires and Control burning Combustion engine vehicles Charbroiled meat Burning or scrap tires

24 Very toxic in the environment- may cause long-term damage BaP is not produced commercially in the United States except as research chemical BaP has decreased it emission over last 13 years Emissions from Prodtion Processes have reduced greatest BaP ENVIRONMENTAL INFORMATION

25 PREVENTIONS Barbecue meat at low temperatures, do not overcook Use thinner slices of meat (they cook faster and with less heat) Turn the meat more frequently Teriyaki sauce or turmeric-garlic sauce before barbeque Marinade before grilling

26 VISITED WEBSITES 1.http://ce.et.tudelft.nl/social/bbq/june2004/rdscn1044.jpg 2.http://www.chez.com/biomar/images/bap.gifhttp://www.chez.com/biomar/images/bap.gif 3.http://www.physchem.ox.ac.uk/MSDS/BE/benzo(a)pyrene.htmlhttp://www.physchem.ox.ac.uk/MSDS/BE/benzo(a)pyrene.html 4.http://www- personal.une.edu.au/~sglover/CHEM303%20Chapter%203%20HTML/sld 015.htmhttp://www- personal.une.edu.au/~sglover/CHEM303%20Chapter%203%20HTML/sld 015.htm 5.http://www- personal.une.edu.au/~sglover/CHEM303%20Chapter%203%20HTML/sld 014.htmhttp://www- personal.une.edu.au/~sglover/CHEM303%20Chapter%203%20HTML/sld 014.htm 6.http://www.naei.org.uk/pollutantdetail.php?poll_id=41&issue_id=2http://www.naei.org.uk/pollutantdetail.php?poll_id=41&issue_id=2 7.http://www.abc.net.au/health/thepulse/s1298158.htm 8.http://www.mybiology.com/chime/dna_bynzopyrene_window.htm 9.http://www.chem.ucalgary.ca/courses/351/Carey5th/Ch15/ch15-3-4.html 10.http://en.wikipedia.org/wiki/Benzopyrenehttp://en.wikipedia.org/wiki/Benzopyrene 11.http://www.nyu.edu/projects/geacintov/http://www.nyu.edu/projects/geacintov/ 12.http://www.nyu.edu/projects/geacintov/WEB_Txt_PAH.htmhttp://www.nyu.edu/projects/geacintov/WEB_Txt_PAH.htm 13.http://ntp.niehs.nih.gov/ntp/roc/eleventh/profiles/s150pah.pdf 14.http://www.mun.ca/biology/scarr/Fig19_26_benzopyrene.gif 15.http://nar.oxfordjournals.org/cgi/content/full/30/23/5284http://nar.oxfordjournals.org/cgi/content/full/30/23/5284 16.http://www.jce.divched.org/HS/Journal/Issues/2004/Feb/abs245.html 17.http://www.personal.une.edu.au/~sglover/CHEM303%20Chapter%203%2 0HTML/img020.gifhttp://www.personal.une.edu.au/~sglover/CHEM303%20Chapter%203%2 0HTML/img020.gif 18.http://www.scorecard.org/chemical- profiles/summary.tcl?edf_substance_id=50-32-8http://www.scorecard.org/chemical- profiles/summary.tcl?edf_substance_id=50-32-8 19.http://www.nyu.edu/projects/geacintov/images/WEB_Figures/WEB_PAH2. jpghttp://www.nyu.edu/projects/geacintov/images/WEB_Figures/WEB_PAH2. jpg 20.http://www.ecgservices.com/beaker.jpg 21.Castellion, Mary and McMurry John. Fundamentals of General, Organic, and Biological Chemistry. Third Edition. New Jersey: Prentice Hall Upper Saddle River, 1999. 22.Tortora, Gerard and Berdell R. Funke and Christine L. Case. Microbiology An Introduction, 8th Edition.


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