Moreover, following transformation with H - Ras, these cells initiated
tumor xenografts in immunocompromised mice with higher efficiency than their epithelial counterparts [5].
In these experiments, Berger and colleagues show that somatic PREX2 mutations identified through whole - genome sequencing of human melanoma can contribute to enhanced lethality of
tumor xenografts in nude mice (Figure 3B, S6B, and S6C; Berger et al., 2012).
Not exact matches
Finally, they were also able to reduce
tumor growth
in their first
in vivo
xenograft analysis.
Additional experiments also showed that TiY can suppress the
tumor growth
in mice
xenograft model.
To overcome these problems, Min and his team developed a new modality to visualize glucose uptake activity inside single cells based on stimulated Raman scattering (SRS) imaging, and demonstrated its use
in live cancer cells,
tumor xenograft tissues, primary neurons and mouse brain tissues.
Terbinafine, a U.S. Food and Drug Administration — approved antifungal drug targeting SQLE, markedly inhibited SQLE - induced NAFLD - HCC cell growth
in NAFLD - HCC and HCC cells and attenuated
tumor development
in xenograft models and
in Sqle transgenic mice.
EZH2 inhibition delayed
tumor onset
in KDM6A - null cells and caused regression of KDM6A - null bladder
tumors in both patient - derived and cell line
xenograft models.
We created a mouse
xenograft model
in which SiHa cervical cancer cells were injected into mice subcutaneously, and the resultant
tumors were treated with PAL three times a week for 6 weeks.
We then usually move onto
xenograft models and then also, if available, try to test some of these compounds
in genetically engineered mouse models that have particular mutations driving
tumor formation.
In a 1988 paper summarizing his findings, Fiebig concluded that
xenograft mice were wonderful models for broadly testing new drugs against human
tumors, but they «can not be used as a clinical routine method» for predicting patient treatment.1 The idea of using
xenograft mice as personal avatars for cancer patients was discarded.
The researchers used an
in vivo model of PARP inhibitor resistance
in patient - derived
tumor xenografts (PDXs).
Personal drug regimens based on
xenograft mice harboring a single patient's
tumor still need to prove their true utility
in medicine.
These days, mice grafted with human
tumors, known as patient - derived
xenograft (PDX) mice, are common
in cancer research laboratories.
Since starting her new role as an investigator
in the In Vivo Pharmacology group at Novartis Oncology, Bhang has been working on using the ClonTracer library to monitor clonal dynamics following drug treatment in cell line and primary tumor xenograft model
in the
In Vivo Pharmacology group at Novartis Oncology, Bhang has been working on using the ClonTracer library to monitor clonal dynamics following drug treatment in cell line and primary tumor xenograft model
In Vivo Pharmacology group at Novartis Oncology, Bhang has been working on using the ClonTracer library to monitor clonal dynamics following drug treatment
in cell line and primary tumor xenograft model
in cell line and primary
tumor xenograft models.
Zebrafish larva implanted with cancer patient's
tumor (red) RITA FIOR / CHAMPALIMAUD CENTRE FOR THE UNKNOWNSee R. Fior et al., «Single - cell functional and chemosensitive profiling of combinatorial colorectal therapy
in zebrafish
xenografts,» PNAS, doi: 10.1073 / pnas.1618389114, 2017
Finally, I have a category of «other cancers» with exomes published
in 2011; these include pancreastic cysts and cell lines, gastric cancer
tumors, and prostate cancer samples derived through mouse
xenograft models.
Comparative genomic hybridization showed a normal pattern
in the first case and a gain of chromosomal 12
in the
xenografted tumor.
In a
xenograft KMT2D - mutated T - lymphoma model, dual treatment with chidamide and decitabine significantly retarded
tumor growth and induced cell apoptosis through modulation of the KMT2D / H3K4me axis.
(G) Immunostaining of p - ERK
in tumor samples of
xenografted murine models bearing KMT2D V5486 mutants treated with CHID and / or DECI.
In - vivo treatments of
xenografted tumors showed significant
tumor growth inhibition induced either by rituximab or gemcitabine alone and an impressive efficacy of combined treatment.
In a series of lab experiments with cell lines, human xenograft tumors in mice and primary human prostate cancer samples, the researchers demonstrated that miR - 34a inhibits prostate cancer stem cells by suppressing CD4
In a series of lab experiments with cell lines, human
xenograft tumors in mice and primary human prostate cancer samples, the researchers demonstrated that miR - 34a inhibits prostate cancer stem cells by suppressing CD4
in mice and primary human prostate cancer samples, the researchers demonstrated that miR - 34a inhibits prostate cancer stem cells by suppressing CD44.
Flavopiridol inhibits several cellular kinases and has demonstrated cytostatic and cytotoxic activity
in vitro and
in vivo
in numerous human
tumor cell lines and
xenograft models (including human breast, prostate, and lung carcinoma) at clinically achievable concentrations.
It was indeed found DAXX promotes the
in vivo tumorigenicity of two human PCa cell lines
in a subcutaneous
tumor xenograft model via suppression of autophagy [Submitted].
Accordingly, p - ERK upregulation was observed not only
in tumor samples of PTCL - NOS patients with KMT2D mutations, but also
in those of
xenografted T - lymphoma mice bearing KMT2D V5486M mutants, the latter being inhibited by combined treatment with chidamide and decitabine (Figure 5F, G).
PP2A mediates diosmin p53 activation to block HA22T cell proliferation and
tumor growth
in xenografted nude mice through PI3K - Akt - MDM2 signaling suppression.
We also found that the EphB4 receptor expressed on the surface of breast cancer cells can promote
tumor xenograft growth by enhancing blood vessel formation through interactions with its preferred ligand, ephrin - B2, present
in tumor endothelial cells.
We have recently reported that the GHRH antagonist, MIA - 602, suppresses the expression of inflammatory cytokines
in human TNBC
tumors xenografted into nude mice.
Acquired
tumor cell resistance to sunitinib causes resistance
in a HT - 29 human colon cancer
xenograft mouse model without affecting sunitinib biodistribution or the
tumor microvasculature
To purify
tumor cells, PC3
xenograft tumors were aseptically dissected out from animals and minced into ∼ 1 - mm3 pieces
in RPMI - 7 % FBS.
Intraperitoneal injection of the HIF - 1α inhibitor, YC1, following
tumor initiation reduces the hypoxic CSC effect
in MCF7
xenografts and results
in no correlation between
xenograft size and MFC (Fig. 5C).
On the contrary, recent evidence indicates that XMRV is a contaminant originating from the recombination of two mouse endogenous retroviruses during passaging of a prostate
tumor xenograft (CWR22)
in mice, generating laboratory - derived cell lines that are XMRV - infected.
A study by Pauli and colleagues
in this issue of Cancer Discovery describes the creation of a precision cancer platform for patients with advanced disease, integrating DNA sequencing of patient
tumors with the generation of patient - derived organoids and
xenografts.
We also demonstrate that immunoglobulin - secreting NSCs exhibit preferential tropism to
tumor cells
in vivo, and can deliver antibodies to human breast cancer
xenografts in mice.
We next tested the ability of antibody - expressing NSCs to deliver anti-HER2 antibodies to
tumor foci
in vivo using a
xenograft nude - beige mouse model.
Importantly, an inverse correlation was observed for ER - α — negative lines with a decrease
in the proportion of MFC within the
xenograft as
tumor size increases (Fig. 5Bii).
ONC201 combined with cytarabine
in a Burkitt's lymphoma
xenograft model induced
tumor growth inhibition that was superior to either agent alone.
A, HIF - 1α and Glut1 expression
in ER - α — positive (i) and negative (ii)
xenografts compared with
tumor size (mm3).
ONC201 combined with bortezomib
in a Burkitt's lymphoma
xenograft model reduced
tumor cell density and improved CHOP induction compared to either agent alone.
Autophagy inhibition synergistically enhances anticancer efficacy of RAMBA, VN / 12 -1
in SKBR - 3 cells, and
tumor xenografts.
This included evaluation of
tumor burden
in mice orthotopically
xenografted, as well as analysis of the overall rate of survival.
Over 170 carefully curated, well - characterized patient - derived
xenograft tumor models are available for use
in your facility, or use Horizon's comprehensive preclinical
in vivo efficacy service.
HCMV and COX - 2 expression correlated
in primary
tumors, cell lines, and medulloblastoma
xenografts.
Sulforaphane, a putative anticarcinogen
in broccoli, was provided orally to mice bearing androgen - insensitive human PC - 3
xenografts, and resulted
in tumor volumes of 207 ± 35 and 90 ± 22 mm3 for the control and sulforaphane groups, respectively (22).