Hypoxia and estrogen are functionally equivalent in breast cancer-endothelial cell interdependence.
about
The Tumor Macroenvironment: Cancer-Promoting Networks Beyond Tumor BedsIdentification of collaborative driver pathways in breast cancer.Combining antiangiogenic therapy with adoptive cell immunotherapy exerts better antitumor effects in non-small cell lung cancer modelsThe histone demethylase enzyme KDM3A is a key estrogen receptor regulator in breast cancer.Luminal breast cancer metastases and tumor arousal from dormancy are promoted by direct actions of estradiol and progesterone on the malignant cellsInduction of cellular prion protein (PrPc) under hypoxia inhibits apoptosis caused by TRAIL treatment.How interacting pathways are regulated by miRNAs in breast cancer subtypes.Estrogen-dependent downregulation of hypoxia-inducible factor (HIF)-2α in invasive breast cancer cellsPLC-β2 is modulated by low oxygen availability in breast tumor cells and plays a phenotype dependent role in their hypoxia-related malignant potential.MicroRNA-135b regulates ERα, AR and HIF1AN and affects breast and prostate cancer cell growthCell density-mediated pericellular hypoxia and the local dynamic regulation of VEGF-a splice variants in ovine ovarian granulosa cells.GPER mediates differential effects of estrogen on colon cancer cell proliferation and migration under normoxic and hypoxic conditions.Estrogen receptor 1 (ESR1) regulates VEGFA in adipose tissue.Macrophage inflammatory factors promote epithelial-mesenchymal transition in breast cancer.Role of TXNDC5 in tumorigenesis of colorectal cancer cells: In vivo and in vitro evidence.Crosstalk between Notch, HIF-1α and GPER in Breast Cancer EMT
P2860
Q26799120-15F5A95A-FD7A-4044-ABD5-92E08055842FQ33953601-460AAC41-2A74-44D0-A237-FF134FEB3888Q34782683-0AA4A89A-F671-48C9-8A58-516FBD3A1B48Q34883436-EE7663DA-76CA-4AFE-92C5-1F188461A25BQ35000639-F5AAFB9E-C750-44B5-9D07-6DC01957466CQ35741681-0AEE7AF4-18EE-4A6A-B4B1-0B807104A9BDQ36276533-9F798887-E5C4-453D-8179-A037B5D4778EQ37327681-76C46A8B-4A8C-4BD0-A61D-E95C9A58AAEEQ40088702-317F610B-4E5F-4ECF-B783-714D8D2ADFD7Q41136545-ACCF5CC2-9B87-40C2-9FF6-2DCF9847EC4BQ42705045-0E3640CE-8231-4FCE-AB45-B8EED09DB579Q45740789-41A4C1C2-97EE-417F-AE77-5AC884A5F08BQ46727445-A3070B27-0B2A-4367-B826-73F97D82F219Q54986341-DA5FC9A8-B967-415D-A187-BD372D2FD8FEQ55496558-A13D24A2-F192-48F5-9703-69AED89EAECCQ57109688-4E717E32-304F-49EB-9A7B-E851DA292F2C
P2860
Hypoxia and estrogen are functionally equivalent in breast cancer-endothelial cell interdependence.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Hypoxia and estrogen are funct ...... othelial cell interdependence.
@ast
Hypoxia and estrogen are funct ...... othelial cell interdependence.
@en
type
label
Hypoxia and estrogen are funct ...... othelial cell interdependence.
@ast
Hypoxia and estrogen are funct ...... othelial cell interdependence.
@en
prefLabel
Hypoxia and estrogen are funct ...... othelial cell interdependence.
@ast
Hypoxia and estrogen are funct ...... othelial cell interdependence.
@en
P2093
P2860
P356
P1433
P1476
Hypoxia and estrogen are funct ...... othelial cell interdependence.
@en
P2093
Abraham Mittleman
Andrea L George
Raj K Tiwari
Robert Suriano
Shilpi Rajoria
P2860
P2888
P356
10.1186/1476-4598-11-80
P577
2012-10-22T00:00:00Z
P5875
P6179
1030889115