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1 dictated by the proliferative status of the tumor-initiating cell.
2 es are separable based on the lineage of the tumor-initiating cell.
3 odulating the lineage potential of MMTV-Wnt1 tumor initiating cells.
4 t in primary CRC, which potentially includes tumor initiating cells.
5 he elimination of undifferentiated stem-like tumor initiating cells.
6 from noisy expression data of CD44+CD24-/low tumor initiating cells.
7 gene target expression segregate to CD133(+) tumor initiating cells.
8 Tetraspanins mark stem cells and tumor initiating cells.
9 operties of 3T3 fibroblasts and glioblastoma tumor initiating cells.
10 nomic profile of residual, therapy resistant tumor initiating cells.
11 nses to NOTCH3 and expands therapy-resistant tumor-initiating cells.
12 ected strategy of immunotherapy to eradicate tumor-initiating cells.
13 ttributed to the presence of CD44-expressing tumor-initiating cells.
14 t attenuation of tumorigenicity by targeting tumor-initiating cells.
15 ewal is thought to be a critical property of tumor-initiating cells.
16 and also has been linked to the capacity of tumor-initiating cells.
17 and lung metastases are highly enriched for tumor-initiating cells.
18 dentify MELK as a potential target in breast tumor-initiating cells.
19 r eradication of primary tumors derived from tumor-initiating cells.
20 hology, suggesting a mixed-lineage origin of tumor-initiating cells.
21 say, a Lin(-)CD29(H)CD24(H) subpopulation of tumor-initiating cells.
22 gating the normal differentiation program of tumor-initiating cells.
23 sis, providing signals that maintain mammary tumor-initiating cells.
24 d in a decline in kynurenine production from tumor-initiating cells.
25 nt of effective therapeutic agents targeting tumor-initiating cells.
26 ed to be resistant to chemotherapy caused by tumor-initiating cells.
27 t Rspo1 and the Sca1-population, enriched in tumor-initiating cells.
28 emalignant cells and activates quiescence in tumor-initiating cells.
29 oRNA-203 promotes selection and expansion of tumor-initiating cells.
30 ions suggest an active selection process for tumor-initiating cells.
31 ignature similar to that observed for human 'tumor-initiating' cells.
32 flammatory cytokine production, and increase tumor-initiating cell abundance and metastatic progressi
33 the effects of Smoothened antagonists on BCC tumor initiating cell and also suggest that currently av
34 evels results in reduced tumor growth, fewer tumor initiating cells and reduced metastasis within the
35 in turn, regulate the relative proportion of tumor initiating cells and the latency of her-2-driven t
36 the mTORC1 kinase induces differentiation of tumor-initiating cells and allows their subsequent deple
37 at the oncofetal protein 5T4 is expressed on tumor-initiating cells and associated with worse clinica
38 cancer models, we found that TcdBFBD reduces tumor-initiating cells and attenuates growth of basal-li
39 mal transition-driving genes, reminiscent of tumor-initiating cells and claudin-low breast cancer.
40 ed endothelial cells (TDECs) originated from tumor-initiating cells and did not result from cell fusi
41 horylated by a Jak2-mediated pathway only in tumor-initiating cells and in human SHH-type medulloblas
42 to maintain proper exon recognition in brain tumor-initiating cells and may provide new inroads for n
43 at the intersections of stem cell function, tumor-initiating cells and multilineage tumor developmen
44 ms by which RA targets GBM-derived stem-like tumor-initiating cells and novel targets applicable to d
45 how that Fzd7 marks a population of putative tumor-initiating cells and that targeting Fzd7 offers a
47 glioblastoma identifies regulators of brain tumor-initiating cells and tumor growth that could serve
49 ined a mixture of red cells (PDGF-expressing/tumor-initiating cells) and green cells (recruited proge
50 iforme (GBM) research is the identity of the tumor-initiating cell, and its contribution to the malig
51 mor cell growth, decreased the proportion of tumor-initiating cells, and decreased tumor formation in
52 resistance, identification of stem cells and tumor-initiating cells, and development of mouse models
53 ) in ovarian cancer cells and ovarian cancer tumor-initiating cells, and that knockdown of SFXN4 inhi
55 and cell deformability, and demonstrate that tumor-initiating cells are less differentiated in terms
58 an prospectively identify glioblastoma brain tumor initiating cells as well as human muscle stem cell
59 ng possibility that these cells could be the tumor-initiating cells, as has been suggested for adult
61 rowth through the generation or expansion of tumor initiating cells bearing stem-like characteristics
63 Breast tumors may derive from self-renewing tumor-initiating cells (BT-ICs), which contribute to tum
65 enic signaling by NOTCH is elevated in brain tumor-initiating cells (BTIC) in malignant glioma, but t
66 bolic dysregulation in patient-derived brain tumor-initiating cells (BTIC) to a nexus between MYC and
69 of the endosomal GTPase Rab35 in human brain tumor initiating cells (BTICs) increases glioblastoma gr
70 to tumor progression by enriching for brain tumor initiating cells (BTICs) owing to preferential BTI
76 e et al. determined that GSI-resistant brain tumor-initiating cells (BTICs) from GBM express a higher
78 both glioma stemlike cells (GSCs) and brain tumor-initiating cells (BTICs) have been implicated in G
80 m cell regulatory pathways to maintain brain tumor-initiating cells (BTICs), also known as cancer ste
81 sub-fraction of cancer cells, termed breast tumor-initiating cells (BTICs), that undergo epithelial
84 duced tumors contained a large percentage of tumor-initiating cells, but these were reduced significa
85 e tumor growth, angiogenesis, metastasis and tumor-initiating cells by in vivo imaging and provide a
89 to the unique properties of iron handling in tumor-initiating cells (cancer stem cells), novel contri
92 Fbeta drives Notch1-mediated EMT to generate tumor initiating cells characterized by high CD44 expres
93 proposed to be composed of two compartments: tumor-initiating cells characterized by a slow and asymm
94 )CXCR4(+) (CXC receptor 4) colorectal cancer tumor-initiating cells (Co-TICs) and the LN stromal micr
97 equired for maintenance of cancer stem cells/tumor-initiating cells (CSCs/TICs), which drive tumorige
98 e showed recently that cancer stem cells, or tumor-initiating cells, derived from human glioblastoma
101 p19(ARF) profoundly influences the nature of tumor-initiating cells during BCR/ABL-mediated leukemoge
103 lineage-associated OLIG2(+) progenitors are tumor-initiating cells during medulloblastoma tumorigene
105 e: Coupling single-cell transcriptomics with tumor-initiating cell enrichment identified IFN response
108 of cancer.(1-4) The nature and existence of tumor-initiating cells for leukemia and other malignanci
109 xenograft growth assays, we determined that tumor initiating cell frequencies approximate one per 1.
111 he growth of a range of tumor types, reduces tumor-initiating cell frequency, and exhibits synergisti
113 ink colitis and cancer identifying potential tumor-initiating cells from colitic patients, suggesting
114 d basal-like TNBC tumors in mice and blocked tumor-initiating cell function and macrometastasis.
115 n expression of antigens thought to identify tumor initiating cells, generation of 3D aggregates when
116 novel HSP90 inhibitor, NVP-HSP990, in glioma tumor-initiating cell (GIC) populations, which are stron
117 t brain tumor, harbors a small population of tumor initiating cells (glioblastoma stem cells) that ha
119 ther tumor cell holoclones genuinely contain tumor-initiating cells has not been directly addressed.
121 , the mechanisms that regulate quiescence in tumor-initiating cells have not been analyzed in detail
122 ulations called cancer stem cells (CSCs), or tumor-initiating cells, have been defined in functional
123 astic modulus induced in 3T3 fibroblasts and tumor initiating cells in response to agents that soften
124 ed in airway epithelial repair that may be a tumor-initiating cell in lung cancer and which may be as
127 tify the entire population of epithelial and tumor-initiating cells in human metastatic colon cancer.
129 However, the precise contribution of CD133+ tumor-initiating cells in mediating colon cancer metasta
131 in signaling can further demarcate high-ALDH tumor-initiating cells in the nondysplastic epithelium o
132 that reparative K14+ progenitor cells may be tumor-initiating cells in this subgroup of smokers with
133 this LEFTY1-BMPR2 interaction is specific to tumor-initiating cells in triple-negative breast cancer
134 erapeutic agents is effective in killing the tumor-initiating cells in vitro and inhibits tumor forma
135 nation in inducing differentiation of breast tumor-initiating cells in vivo Furthermore, gene express
136 astasis, and recurrence, and targeting these tumor-initiating cells is necessary to eradicate tumors.
137 Although the role of CD271 as a marker of tumor-initiating cells is still a matter of debate, its
138 that human malignant glioma tissues and also tumor-initiating cells isolated from fresh human maligna
139 eficiencies) that were derived from CD44(hi) tumor-initiating cells isolated from PCa-20a cells.
142 ve and tumorigenic capacities of the mammary tumor-initiating cells (MaTICs) of claudin-low breast ca
143 val in brain tumors and other cancers; thus, tumor initiating cells may extract nutrients with high a
144 in pre-malignant DCIS lesions and that these tumor-initiating cells may determine the phenotype of DC
145 e viability and maintenance of self-renewing tumor-initiating cells may ultimately lead to improved t
147 livary gland imaginal ring, we find that the tumor-initiating cells normally undergo endoreplication
148 nd by increased reliance of cancer cells and tumor-initiating cells on mitochondria, resulting in pot
149 od that enriches cancer stem cells (CSCs) or tumor-initiating cells on the basis of cell adhesion pro
150 renewing, and highly metastatic cells called tumor initiating cells or cancer stem cells (CSCs).
151 for tumor initiation and propagation, termed tumor initiating cells or cancer stem cells (CSCs).
154 n epithelial-to-mesenchymal transition and a tumor initiating cell phenotype, and that it is required
155 PKCiota-ELF3-NOTCH3 signaling controls the tumor-initiating cell phenotype by regulating asymmetric
156 the Lin(-)CD29(H)CD24(H) mouse mammary gland tumor-initiating cell population include those involved
158 arker for distinct subsets of chemoresistant tumor-initiating cell populations in diverse human malig
160 pigenomic profiling revealed that IFE and HF tumor-initiating cells possess distinct chromatin landsc
164 r subpopulation, termed cancer stem cells or tumor-initiating cells, promotes therapeutic resistance
166 uding glioma stem cells (GSC), which are the tumor-initiating cells responsible for treatment failure
167 tumors, which are driven by a component of 'tumor-initiating cells' retaining stem cell properties.
168 enuate cancer stem cell markers, inhibit the tumor-initiating cell's neurosphere-forming capacity, an
169 ddition to angiogenic effects, VEGF promotes tumor-initiating cell self-renewal through VEGFR-2/STAT3
170 rt differential drug sensitivity, indicating tumor-initiating cell states and genetic drivers dictate
171 Here we showed that the basal cell carcinoma tumor-initiating cell surface protein CD200, through ect
172 140/SOX2 pathway critically regulates breast tumor-initiating cell survival, providing a new link bet
173 ribe the isolation and characterization of a tumor-initiating cell (T-IC) subpopulation in primary hu
174 t evidence has demonstrated the existence of tumor-initiating cells (T-ICs) as the culprit for treatm
175 r can arise from a cancer stem cell (CSC), a tumor-initiating cell that has properties similar to tho
176 Human melanomas contain a population of tumor-initiating cells that are able to maintain the gro
177 existence of a small population of CD133(+) tumor-initiating cells that are capable of regenerating
178 own about chromatin mechanisms that regulate tumor-initiating cells that are proposed to be responsib
179 fectively eliminate the subpopulation of GBM tumor-initiating cells that are responsible for relapse.
180 mor growth in vivo, decreasing the number of tumor-initiating cells, thus supporting its pro-oncogeni
181 The effectiveness of CD133NPs in reducing tumor initiating cell (TIC) fraction was investigated us
182 s leads to an induction of a CD24(-)/CD44(+) tumor initiating cell (TIC) population (4) sGRP78(+) bre
183 in pancreatic cancer along with a decreased tumor initiating cell (TIC) population in pancreatic tum
186 al-mesenchymal transition (EMT), promoting a tumor-initiating cell (TIC) phenotype characterized by i
187 sition reversibly between slow-proliferating tumor-initiating cells (TIC) and their differentiated, f
190 y of continuous culture models and human GBM tumor-initiating cells (TIC) in both Boyden chamber and
193 Understanding the mechanisms supporting tumor-initiating cells (TIC) is vital to combat advanced
196 Emerging evidence indicates the presence of tumor-initiating cells (TIC) or cancer stem cells in ost
198 ypothesis that HER2/HER3 signaling in breast tumor-initiating cells (TIC) promotes self-renewal and s
200 play cellular hierarchies with self-renewing tumor-initiating cells (TIC), also known as cancer stem
201 y organized and driven by a subpopulation of tumor-initiating cells (TIC), or cancer stem cells.
202 P) cells showed up to a 3-fold enrichment of tumor-initiating cells (TIC), suggestive of a sanctuary
210 (RTK)/RAS signaling can lead to outgrowth of tumor-initiating cells (TICs) and drive therapeutic resi
211 ene expression signatures derived from human tumor-initiating cells (TICs) and human mammary stem cel
212 s by activating JAK/STAT signaling in breast tumor-initiating cells (TICs) and promoted TIC self rene
213 east cancer cells bearing characteristics of tumor-initiating cells (TICs) and that strongly associat
220 rogression in cancer requires populations of tumor-initiating cells (TICs) endowed with unlimited sel
222 (MECs) to mammary stem cells (MaSCs) and to tumor-initiating cells (TICs) have not been entirely elu
224 dentification of therapeutic targets against tumor-initiating cells (TICs) is a priority in the devel
226 ucing kinase (NIK), support the expansion of tumor-initiating cells (TICs) that copurify with a CD24(
227 , and treatment resistance is potentiated by tumor-initiating cells (TICs) that thrive under hypoxia.
228 Moreover, GDF15 induces the expansion of MM tumor-initiating cells (TICs), and changes in the serum
229 of cancer in which only a fraction of cells, tumor-initiating cells (TICs), can sustain tumor growth.
230 lentiviral particles, and transduction into tumor-initiating cells (TICs), followed by in vivo trans
231 o has therapeutic implications for targeting tumor-initiating cells (TICs), the tumor stroma, and che
232 oncogene-induced expansion and activities of tumor-initiating cells (TICs), whereas it is largely dis
233 njury and establishes selective pressure for tumor-initiating cells (TICs), which proliferate to form
245 ds on a small subset of tumor cells, called "tumor-initiating cells" (TICs), with SC-like properties.
246 inhibition of SOS1 reduced the frequency of tumor-initiating cells to curb spheroid growth in situ a
248 C receptors by ligands BDNF and NT3 enhances tumor-initiating cell viability through activation of ER
249 that breast cancer is derived from a single tumor-initiating cell with stem-like properties, but the
251 Within established GBM, a subpopulation of tumor-initiating cells with stem-like properties (GBM st
252 ver, interaction of accessory cells with the tumor-initiating cell within the microenvironment is oft