Tumor microenvironment abnormalities: Causes, consequences, and strategies to normalize
By Dai Fukumura, Rakesh K. Jain. Journal of Cellular Biochemistry, 2007
600 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/ca5c2b9162ab4eea94830d53318e531cb9e531e7
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- Dai Fukumura
- Rakesh K. Jain
- M. Swartz
- H. Wiig
- C. Roma-Rodrigues
- Alexandra R. Fernandes
- R. Mendes
- Pedro Viana Baptista
In Molecular Biology
- Dai Fukumura
- Rakesh K. Jain
- H. Wiig
- M. Swartz
- Pedro Viana Baptista
- Alexandra R. Fernandes
- C. Roma-Rodrigues
- R. Mendes
In Oncology
- Dai Fukumura
- H. Wiig
- Rakesh K. Jain
- M. Swartz
- C. Roma-Rodrigues
- Alexandra R. Fernandes
- R. Mendes
- Pedro Viana Baptista
Citations in the corpus
- Tumor microvasculature and microenvironment: targets for anti-angiogenesis and normalization. (2007, background): “Interstitial Hypertension and Abnormal Lymphatics in Tumors Both animal and human tumors exhibit interstitial hypertension while the interstitial fluid pressure (IFP) in normal tissues is around zero mmHg (Fukumura and Jain, 2007; Jain et al., 2007).”
- Interstitial fluid and lymph formation and transport: physiological regulation and roles in inflammation and cancer. (2012, background): “As recently summarized (142, 187, 221), there are several factors that contribute to the high Pif in tumors.”
- Digoxin and other cardiac glycosides inhibit HIF-1α synthesis and block tumor growth (2008, neutral): “M human cancers contain regions of hypoxia because of rapid cell proliferation and the presence of intratumoral blood vessels that are structurally and functionally abnormal, resulting in both spatial and temporal heterogeneity of blood flow (1, 2).”
- Targeting Tumor Microenvironment for Cancer Therapy (2019, background): “Bevacizumab (Avastin), an antibody that targets VEGF, was the first anti-angiogenic approved by FDA that is already in the clinics [62].”