2006•Unpublished venueRequires access

Expression of distal (testis) promoter of EDAG in leukemia cell lines and its regulation during cell differentiation

WU Ke-f

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Abstract

Objective To explore the regulation mechanism of EDAG expression in leukemia cells. Methods We detected the pattern of EDAG-t mRNA expression via RT-PCR in a panel of leukemia cell lines. Then we further explored the regulation of EDAG-t and EDAG-h expression during the differentiation of K562 and U937 cells. Results EDAG-t (human HEMGN-t) isoform could also be detected in the leukemia cell lines K562 and U937. And both HEMGN-t and HEMGN-h could be down regulated during the differentiation of K562 and U937 cells but the kinetics were different. Conclusion The regulatory mechanisms for HEMGN-t in testis and leukemia cell lines deserve further investigation.

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What this paper is about

Objective To explore the regulation mechanism of EDAG expression in leukemia cells. Methods We detected the pattern of EDAG-t mRNA expression via RT-PCR in a panel of leukemia cell lines. Then we further explored the regulation of EDAG-t and EDAG-h expression during the differentiation of K562 and U937 cells. Results EDAG-t (human HEMGN-t) isoform could also be detected in the leukemia cell lines K562 and U937. And both HEMGN-t and HEMGN-h could be down regulated during the differentiation of K562 and U937 cells but the kinetics were different. Conclusion The regulatory mechanisms for HEMGN-t in testis and leukemia cell lines deserve further investigation.

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Available abstract

Objective To explore the regulation mechanism of EDAG expression in leukemia cells. Methods We detected the pattern of EDAG-t mRNA expression via RT-PCR in a panel of leukemia cell lines. Then we further explored the regulation of EDAG-t and EDAG-h expression during the differentiation of K562 and U937 cells. Results EDAG-t (human HEMGN-t) isoform could also be detected in the leukemia cell lines K562 and U937. And both HEMGN-t and HEMGN-h could be down regulated during the differentiation of K562 and U937 cells but the kinetics were different. Conclusion The regulatory mechanisms for HEMGN-t in testis and leukemia cell lines deserve further investigation.

Key concepts: K562 cells, U937 cell, Leukemia, Cell culture, Cellular differentiation, Biology, Cell, Molecular biology

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