ライフサイエンスコーパス: low metastatic

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1 ly expressed in melanoma cells with high vs. low metastatic abilities.

2 vels in human colon cancer cells of high and low metastatic ability were manipulated via expression o

3 noma variants, SBC-2 (nonmetastatic), A375P (low metastatic), and A375SM (high metastatic), by increa

4 l implanted with high metastatic (B16F10) or low metastatic (B16F1) melanoma cells.

5 evels, which predicts their inherent high or low metastatic capacity.

6 ities of IL-8 and remain unmethylated in the low metastatic cell lines where the IL-8 gene is relativ

7 erences in IL-8 release between the high and low metastatic cell lines.

8 RNA transcripts than parental PC-3M cells or low metastatic cells, which displayed a heterogeneous pa

9 d2 and low SEMA3F levels compared with their low metastatic counterparts.

10 gments (OPN-5 kDa, residues 167-210) induced low-metastatic HCC cellular invasion via CD44 receptors,

11 e in vivo behavior of a variety of high- and low-metastatic human and mouse cancer cell lines and the

12 31 cells than in distal non-tumor tissue and low-metastatic MCF-7 cells, respectively.

13 ich was abrogated by silencing CCN1/CYR61 in low metastatic melanoma cells.

14 a cell lines that have been characterized as low metastatic or high metastatic, respectively, for AP-

15 ly metastatic cells were compared with their low metastatic parental cells (686LN-Ps), we found that

16 GF, type IV collagenase, and mdr-1 mRNA than low metastatic parental cells in the same site.

17 3 to a 2-fold greater extent than mucin from low-metastatic parental cell line LS174T.

18 uppressed the growth of Lewis lung carcinoma-low metastatic phenotype metastases in C57BL/6 mice by g

19 d the growth of primary Lewis lung carcinoma-low metastatic phenotype tumors.

20 ular and cell surface galectin 3 in cells of low metastatic potential (LS174T).

21 quate tumor control for iris melanoma with a low metastatic potential of 1% at 7 years.

22 tection of biologically indolent tumors with low metastatic potential.

23 lin E and FAK when compared to tumors with a low metastatic potential.

24 phaM cells produced slow growing tumors with low metastatic potential.

25 atic MDA-MB-435 cells, but not in cells with low metastatic potential.

26 melanomas to prognostic subgroups: class 1 (low metastatic risk) and class 2 (high metastatic risk).

27 s are associated with prolonged survival and low metastatic risk, SF3B1-mutated tumors are associated

28 mall renal masses are indolent and possess a low metastatic risk.

29 REST knockdown in low-metastatic T47D cells and nontumorigenic MCF12A cell

30 Furthermore, ectopic expression of Id2 in low metastatic tumor cells downregulated SEMA3F and, as

31 In contrast, no increase was observed in low-metastatic TXM-40 cells.

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