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1 tiation, transformation, tumorigenicity, and metastatic potential.
2 form secondary tumors, and possess increased metastatic potential.
3 in terms of predictability, complexity, and metastatic potential.
4 histopathology, cytogenetic complexity, and metastatic potential.
5 , CTC clusters have 23- to 50-fold increased metastatic potential.
6 portant biomarkers of cancer progression and metastatic potential.
7 ial depletion of Dicer, can promote enhanced metastatic potential.
8 as possible markers for disease relapse and metastatic potential.
9 witch that confers cancer cells an increased metastatic potential.
10 AC cells and Suit2 derivatives with enhanced metastatic potential.
11 ells with stem-cell-like properties and high metastatic potential.
12 fer aberrant proliferative, survival, and/or metastatic potential.
13 kers or differentiation is the best guide to metastatic potential.
14 ungs of nude mice, suggesting an increase in metastatic potential.
15 ssor whose loss is associated with increased metastatic potential.
16 ns may dysregulate miRNAs, in turn affecting metastatic potential.
17 ndependent growth in soft agar, and enhanced metastatic potential.
18 he adrenal gland, suggesting their increased metastatic potential.
19 erivative of MCF10a cells selected for their metastatic potential.
20 n vimentin is observed, indicating increased metastatic potential.
21 r samples and its expression correlated with metastatic potential.
22 aster entry velocities than cells with lower metastatic potential.
23 as a potential factor that influences brain metastatic potential.
24 n be mechanistically coupled to greater bone metastatic potential.
25 umour adaptation, therapeutic resistance and metastatic potential.
26 s, a property that correlates with increased metastatic potential.
27 ers and suggested to serve as a barometer of metastatic potential.
28 ligand (FasL) and show high malignancy with metastatic potential.
29 tumor might serve as a prognostic marker for metastatic potential.
30 susceptibility to anoikis and impairs their metastatic potential.
31 significant effect on both tumor growth and metastatic potential.
32 rade tumors from high-grade tumors with high metastatic potential.
33 wth, it had a dramatic effect on spontaneous metastatic potential.
34 ansport barriers, and the tumor invasive and metastatic potential.
35 y enhance chemotaxis to HRGbeta1 and overall metastatic potential.
36 STAT1 in STS cells, thereby increasing their metastatic potential.
37 smaller tumors that exhibited an attenuated metastatic potential.
38 aling, neovascularization, invasiveness, and metastatic potential.
39 thelial cells and potentially reducing their metastatic potential.
40 elate with prostate tumor aggressiveness and metastatic potential.
41 hyme (EMT) transition and possible increased metastatic potential.
42 olon cancer, whereas PRL-3 knockdown reduced metastatic potential.
43 of detached breast tumor cells and enhances metastatic potential.
44 A shape its genetic landscape and define its metastatic potential.
45 f deregulated growth, survival and increased metastatic potential.
46 ammary tumor cell lines that differ in their metastatic potential.
47 hology of cancer cells associated with their metastatic potential.
48 did not correlate with either tumor size or metastatic potential.
49 expression, in close agreement with observed metastatic potential.
50 which selects for tumor cells with increased metastatic potential.
51 tumor progression to malignancy and increase metastatic potential.
52 he behaviors of cancer cells associated with metastatic potential.
53 vels could be used as a predictive marker of metastatic potential.
54 umor phenotype, particularly with respect to metastatic potential.
55 astasis and provides potential biomarkers of metastatic potential.
56 ion of biologically indolent tumors with low metastatic potential.
57 ations to promote their growth, survival and metastatic potential.
58 mechanism whereby cancer stem cells acquire metastatic potential.
59 omic instability and aggressive disease with metastatic potential.
60 lls profoundly inhibited their migratory and metastatic potential.
61 sis we show that knockdown of Kdm3a enhances metastatic potential.
62 av1 in HCC cells enhances their invasive and metastatic potential.
63 tumors with shorter latency and have higher metastatic potential.
64 nal consequences on tumor cell signaling and metastatic potential.
65 gression from benign to invasive stages with metastatic potential.
66 elerated mammary tumorigenesis with enhanced metastatic potential.
67 s quantified by a key parameter of intrinsic metastatic potential.
68 oor prognosis due to its highly invasive and metastatic potential.
69 (MCC), an aggressive skin cancer with a high metastatic potential.
70 ells with increased stem cell properties and metastatic potential.
71 conventional anticancer treatments and high metastatic potential.
72 through multiple passages, and tumors retain metastatic potential.
73 tion and invasion in cancer cells to promote metastatic potential.
74 the most prevalent invasive malignancy with metastatic potential.
75 a major biological correlate of breast tumor metastatic potential.
76 tumor growth, apoptotic resistance and high metastatic potential.
77 endow rare cells within a primary tumor with metastatic potential.
78 lines induced AnR and dramatically increased metastatic potential.
79 ntributing to acquisition and maintenance of metastatic potential.
80 where its expression correlated with reduced metastatic potential.
81 from the immune system, and facilitate their metastatic potential.
82 t, histological appearance, invasiveness and metastatic potential.
83 development or abnormal cells as they evolve metastatic potential.
84 of mammary tumor cell lines with increasing metastatic potentials.
85 p63 led to both rapid tumour development and metastatic potential, although the incidence of metastas
86 tant lung adenocarcinoma cell line with high metastatic potential and an orthotopic syngeneic mouse m
87 he most frequently occuring skin cancer with metastatic potential and can manifest rapidly as a commo
88 progression and poor prognosis by increasing metastatic potential and drug resistance in breast cance
89 nt neoplasm of melanocytes with considerable metastatic potential and drug resistance, explaining the
92 ed in pancreatic cancer cell lines with high metastatic potential and human pancreatic tumors compare
93 d isogenic tumor cells, cells with different metastatic potential and malignant vs normal cells can b
94 nt models to assess the impact of surgery on metastatic potential and may guide optimal timing of tre
96 pression and transcriptional activities with metastatic potential and poor prognosis in cancer, altho
97 pressure has been associated with increased metastatic potential and poor prognosis in some tumors.
98 sine kinase ErbB-2 are characterized by high metastatic potential and poor prognosis, but the signali
99 on of Phip in melanoma cell lines suppressed metastatic potential and prolonged the survival of tumor
102 en procoagulant function strongly influences metastatic potential and suggest that endothelial cell-a
103 t when activated in cancer endows cells with metastatic potential and the properties of stem cells.
104 er Notch signaling correlates with increased metastatic potential and worse disease survival rates.
105 ategorizes melanoma specimens based on their metastatic potential and, importantly, is capable of str
106 espect to their infiltrative growth pattern, metastatic potential, and altered cell differentiation b
107 renewability, multipotency, drug resistance, metastatic potential, and enrichment of a metastasis-ass
108 ors positively correlate with cell motility, metastatic potential, and grade, including bladder, mela
109 rcinomas (SCC) is characterized by increased metastatic potential, and SCC progression is associated
110 and MCF-7) with distinct deformabilities and metastatic potentials, and (ii) a heterogeneous breast c
111 motherapy and the acquisition of invasive or metastatic potential, arose within detectable subclones
113 evidence in line with autopsy data that the metastatic potential, as shown by the incidence of CUP,
114 novel integrated perspective on the enhanced metastatic potential associated with MUC16 overexpressio
115 d L-selectin ligand may explain the enhanced metastatic potential associated with tumor cell CEA over
116 to a group of benign fibrous growths without metastatic potential but with a significant risk of loca
117 only a surface marker for cells with higher metastatic potential, but also functionally involved in
118 er stem cells (CSC) appear to have increased metastatic potential, but mechanisms underlying this are
119 trol of cytoplasmic and extracellular pH and metastatic potential, but the isoforms involved and the
120 ased proliferation, decreased apoptosis, and metastatic potential by conservation of proteins like ep
121 ogram to promote survival, proliferation and metastatic potential by mechanisms that remain largely u
126 d with longer glycopolymers showed increased metastatic potential, enhanced cell cycle progression, a
127 t mass, we find that cells possessing higher metastatic potential exhibit faster entry velocities tha
128 onally find that some cell types with higher metastatic potential exhibit greater than expected chang
129 teosarcoma cell lines that exhibit disparate metastatic potential for differences in epigenetic modif
130 but aggressive cutaneous neoplasm with high metastatic potential, has a poor prognosis at late stage
132 n in vitro and significantly reduced in vivo metastatic potential in a preclinical model of experimen
133 fter arterial injury and markedly diminished metastatic potential in a setting of experimental tumor
138 ti-cellular aggregates (MCAs), of increasing metastatic potential in different elastic moduli of hydr
140 tivation may contribute to tumorigenesis and metastatic potential in human cancers via a similar mech
141 apeutic resistance also correlates with high metastatic potential in human cancers, including breast
142 reased tumor growth, tumor angiogenesis, and metastatic potential in many malignancies, including pan
143 ong correlation between NFAT1 expression and metastatic potential in melanoma cell lines and tumor sp
144 that syndecan 1 and 4 correlate to increased metastatic potential in melanoma patients and are an imp
147 3b/27b/24 cluster is found to correlate with metastatic potential in mouse and human breast cancer ce
150 h the markers Sca1 and CD24 are enriched for metastatic potential in orthotopic transplantation assay
151 ial for identifying cell subpopulations with metastatic potential in primary tumors or with resistanc
153 hymal transition with highly tumorigenic and metastatic potential in vivo compared to conventional tw
154 acity during reoxygenation in vitro and lung metastatic potential in vivo On a mechanistic level, we
155 ack PTPN12 exhibited reduced tumorigenic and metastatic potential in vivo that correlated with their
156 dulating Cnot2 expression changes tumor cell metastatic potential in vivo, supporting a functional ro
157 gration of melanoma cells in vitro and their metastatic potential in vivo, whereas miR-182 down-regul
172 ma xenografts that spanned the full range of metastatic potential measured by an in vivo lung colony
173 nd the induction of apoptosis; (b) decreased metastatic potential mediated by down-regulation of the
174 ificantly rescued the decreased invasive and metastatic potential mediated by RSK2 knockdown in vitro
175 o report that the oncogene RhoC, a driver of metastatic potential, modulates glutamine and N-acetylas
179 portant role in controlling invasiveness and metastatic potential of breast cancer cells and that its
180 DNA damage-induced apoptosis and enhance the metastatic potential of breast cancer cells through repr
183 eta-regulated "metastamir" that enhanced the metastatic potential of breast cancers by promoting epit
184 -MEA effectively attenuated the invasive and metastatic potential of cancer cells in vitro and in viv
185 in stem cell pluripotency and suppresses the metastatic potential of cancer cells through multiple me
187 ted by MAPK, the increased cell motility and metastatic potential of cancer cells with PI3K and/or MA
194 chanical phenotypes can be used to grade the metastatic potential of cell populations with the potent
197 particular, miR-200a is likely to affect the metastatic potential of cervical cancer cells by coordin
199 ession of NFATc1 significantly increased the metastatic potential of colon cancer cells, whereas inhi
202 mportance of clonal variation in determining metastatic potential of colorectal cancer cells using th
205 present study, we aimed to evaluate the anti-metastatic potential of deguelin in vivo and in tumor gr
206 y been linked to cellular transformation and metastatic potential of epithelial cancers, our findings
208 RSK2 substantially reduced the invasive and metastatic potential of HNSCC cells in vitro and in vivo
209 rin-A3 and novel EFNA3 lncRNAs increased the metastatic potential of human breast cancer cells, possi
211 channels (VGSC) have been implicated in the metastatic potential of human breast, prostate, and lung
212 11 depletion on the tumorigenic capacity and metastatic potential of human cancer cells and xenograft
213 sublethal dose of radiation can enhance the metastatic potential of human cervical cancer cells via
214 ealed that Hunk is sufficient to restore the metastatic potential of Hunk-deficient tumor cells, as w
215 on in tumors markedly reduces the number and metastatic potential of infiltrating tumor-associated ma
216 significantly abrogated the tumorigenic and metastatic potential of invasive breast cancer cells.
217 mpaired cell migration in vitro and also the metastatic potential of invasive lung cancer cells in vi
218 zygous mutation of Dpc4/Smad4 attenuates the metastatic potential of Kras(G12D/+);Trp53(R172H/+) panc
224 migration/invasion capacity in vitro and the metastatic potential of MDA-MB-231 cells in immunodefici
225 f blueberry phytochemicals on the growth and metastatic potential of MDA-MB-231 cells through modulat
226 showing that interstitial flow increases the metastatic potential of MDA-MB-435S melanoma cells.
229 topaxin reverted the invasive phenotypes and metastatic potential of metastatic HCC cells through reg
232 portant for maintaining the invasiveness and metastatic potential of non-epithelial sarcoma cells.
233 rgistically and is sufficient to promote the metastatic potential of nonmetastatic cells to that of n
234 on in osteosarcoma, thus contributing to the metastatic potential of osteosarcoma cells by altering t
236 oduction correlated with the increase in the metastatic potential of PC-3 and LNPCa prostate cancer m
240 n and messenger RNA were associated with the metastatic potential of PDAC cell lines and progression
241 syltransferase, which is associated with the metastatic potential of PDAC tumors in mice and progress
242 truncated PDGFRalpha is able to restore bone-metastatic potential of prostate cancer cells as effecti
245 these targets in isolation did not alter the metastatic potential of sarcoma cells injected orthotopi
246 tion identifies metastatic cells; rather the metastatic potential of several ROS-generating mutations
247 enewal, gene expression, tumorigenicity, and metastatic potential of spheres at generations G1-G5 wer
248 sion levels did not change with the invasive/metastatic potential of the cancer cells or tumors.
252 In addition, silencing of RSK1 enhanced the metastatic potential of these cells in vivo using a zebr
254 coexist in SCC and that tumor initiation and metastatic potential of these populations can be uncoupl
255 anced the chemosensitivity and decreased the metastatic potential of this p53(null) claudin-low tumor
256 proliferation, migration, invasion, and the metastatic potential of tumor cells by promoting loss of
257 s been shown to enhance the invasiveness and metastatic potential of tumor cells by regulating the ge
258 of action by which kisspeptins suppress the metastatic potential of tumor cells lacking expression o
271 associated with tumor cell invasiveness and metastatic potential, prominent characteristics of NPC.
274 bpd null mammary tumours, which have reduced metastatic potential, show altered expression of inflamm
275 verexpressed specifically in cells with high metastatic potential, suggesting a role for this miRNA a
276 tumor that has a worse prognosis and higher metastatic potential than its adenocarcinoma counterpart
277 evalent, CTC clusters appear to have greater metastatic potential than single CTCs in the circulation
279 pendymoma is a locally aggressive tumor with metastatic potential that arises in diverse locations th
280 fluidity as a necessary cellular feature of metastatic potential that can be controlled by many curr
281 motility, tissue invasion and acquisition of metastatic potential through the upregulation of epithel
282 een resistance to mTOR inhibition and cancer metastatic potential, thus enhancing our understanding o
283 erived exosomes have the ability to transfer metastatic potential to a recipient cell and cancer exos
286 these functional domains in cancer biology, metastatic potential was evaluated in TM(Pro) mice expre
291 bladder carcinoma cell lines with differing metastatic potential were uncoupled from binding to targ
292 n, Stat3 signaling, tumor proliferation, and metastatic potential when expressed in a murine RMS cell
293 mors appear to have had a biologic impact on metastatic potential, whereas mutations arising in the m
294 linked with the expansion of subclones with metastatic potential which we can detect in the blood.
295 r (TNBC) is notoriously aggressive with high metastatic potential, which has recently been linked to
296 B-231 and BT-549 cancer cells stimulated the metastatic potential while it actually inhibited it in t
297 exhibited a slower growth rate and a reduced metastatic potential with a more differentiated epitheli
298 a malignancy characterized by high invasive/metastatic potential, with no efficient therapy after me
300 ve or minimally invasive prediction of tumor metastatic potential would facilitate individualized can
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