Abstract
Estrogens, a group of steroid compounds functioning as the primary female sex hormone, play an important role in the development and progression of breast cancer. In this study, using a novel annealing control primer-based GeneFishing PCR technology, five differentially expressed genes (DEGs), expressed using 10 nM mitogenic estrogens, 17β-estradiol (E2) and 16α-hydroxyestrone (16α-OHE1), were selected from the estrogen receptor (ER)-positive MCF-7 human breast cancer cells. The DEGs, MRPL42, TUBA1B, SSBP1, KNCT2, and RUVBL1, were identified by comparison with the known genes via direct sequencing and sequence homology search in BLAST. Quantitative real-time PCR data showed that two DEGs, tubulin α1b and kinetochore associated 2, were greater than 2-fold upregulated by E2 or 16α-OHE1. Both genes could be new biomarkers for the treatment and prognosis of cancers, and further study may provide insights into the molecular mechanisms underlying development and progression of breast cancer.
| Original language | English |
|---|---|
| Pages (from-to) | 1-6 |
| Number of pages | 6 |
| Journal | Journal of Applied Biological Chemistry |
| Volume | 51 |
| Issue number | 1 |
| DOIs | |
| State | Published - 2008.02.29 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- 16α-hydroxyestrone
- 17β-estradiol
- Breast cancer cells
- Differentially expressed genes
- Estrogen receptor-positive MCF-7 human
- Kinetochore associated 2
- Tubulin αlb
Fingerprint
Dive into the research topics of 'Identification of genes differentially expressed in the MCF-7 cells treated with mitogenic estrogens'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver