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Re: Arsenic in foods

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--- In , Al Pater <old542000@...>

wrote:

>

> Hi All,

>

> It seems that sea-foods have considerable levels of arsenic.

>

> ``Foods of marine origin are very rich in arsenic. Many species of

bony fish contain

> 2 to 8 ppm, oysters 3 to 10 ppm and mussels as high as 120 ppm of

arsenic. Chemical

These levels of arsenic may not be a bad thing, and could suppress

cancer, arguing once again for moderation in all things:

http://tinyurl.com/jtogq

Arsenic inhibition of telomerase transcription leads to genetic

instability

Wen-Chien Chou1, Anita L. Hawkins2, F. Barrett3, Constance A.

2,4 and Chi V. Dang1,3,4

Arsenic is effective in the treatment of acute promyelocytic

leukemia. Paradoxically, it is also carcinogenic. In the process of

elucidating a mechanism of arsenic resistance in a leukemia cell

line, NB4, we discovered that arsenic exposure causes chromosomal

abnormalities, with a preponderance of end-to-end fusions. These

chromosomal end fusions suggested that telomerase activity may be

inhibited by arsenic. We found that arsenic inhibits transcription

of the hTERT gene, which encodes the reverse transcriptase subunit

of human telomerase. This effect may in part be explained by

decreased c-Myc and Sp1 transcription factor activities. Decreased

telomerase activity leads to chromosomal end lesions, which promote

either genomic instability and carcinogenesis or cancer cell death.

These phenomena may explain the seemingly paradoxical carcinogenic

and antitumor effects of arsenic.

Mike

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Guest guest

--- In , Al Pater <old542000@...>

wrote:

>

> Hi All,

>

> It seems that sea-foods have considerable levels of arsenic.

>

> ``Foods of marine origin are very rich in arsenic. Many species of

bony fish contain

> 2 to 8 ppm, oysters 3 to 10 ppm and mussels as high as 120 ppm of

arsenic. Chemical

These levels of arsenic may not be a bad thing, and could suppress

cancer, arguing once again for moderation in all things:

http://tinyurl.com/jtogq

Arsenic inhibition of telomerase transcription leads to genetic

instability

Wen-Chien Chou1, Anita L. Hawkins2, F. Barrett3, Constance A.

2,4 and Chi V. Dang1,3,4

Arsenic is effective in the treatment of acute promyelocytic

leukemia. Paradoxically, it is also carcinogenic. In the process of

elucidating a mechanism of arsenic resistance in a leukemia cell

line, NB4, we discovered that arsenic exposure causes chromosomal

abnormalities, with a preponderance of end-to-end fusions. These

chromosomal end fusions suggested that telomerase activity may be

inhibited by arsenic. We found that arsenic inhibits transcription

of the hTERT gene, which encodes the reverse transcriptase subunit

of human telomerase. This effect may in part be explained by

decreased c-Myc and Sp1 transcription factor activities. Decreased

telomerase activity leads to chromosomal end lesions, which promote

either genomic instability and carcinogenesis or cancer cell death.

These phenomena may explain the seemingly paradoxical carcinogenic

and antitumor effects of arsenic.

Mike

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