Acidic pH enhances the invasive behavior of human melanoma cells

被引:421
作者
MartinezZaguilan, R
Seftor, EA
Seftor, REB
Chu, YW
Gillies, RJ
Hendrix, MJC
机构
[1] ST LOUIS UNIV,SCH MED,PEDIAT RES INST,DEPT PEDIAT,ST LOUIS,MO 63110
[2] UNIV ARIZONA,ARIZONA HLTH SCI CTR,DEPT BIOCHEM,TUCSON,AZ
[3] UNIV ARIZONA,ARIZONA HLTH SCI CTR,CANC BIOL PROGRAM,TUCSON,AZ
关键词
fluorescence; FURA-2; intracellular Ca2+; intracellular pH; invasion; melanoma; SNARF-1;
D O I
10.1007/BF00121214
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As a consequence of poor perfusion and elevated acid production, the extracellular pH (pH(ex)) of tumors is generally acidic, Despite this, most in vitro experiments are still performed at the relatively alkaline pH(ex) of 7.4, This is significant, because slight changes in pH(ex) can have profound effects on cell phenotype, In this study we examined the effects of mildly acidic conditions on the in vitro invasive potential of two human melanoma cell lines: the highly invasive C8161, and poorly invasive A375P, We observed that culturing of either cell line at acidic pH (6.8) caused dramatic increases in both migration and invasion, as measured with the Membrane Invasion Culture System (MICS), This was not due to a direct effect of pH on the invasive machinery, since cells cultured at normal pH (7.4) and tested at acidic pH did not exhibit increased invasive potential, Similarly, cells cultured at acidic pH were more aggressive than control cells when tested at the same medium pH, These data indicate that culturing of cells at mildly acidic pH induces them to become more invasive, Since acid pH will affect the intracellular pH (pH(in)) and intracellular calcium ([Ca2+](in)), we examined the effect of these parameters on invasion, While changes in [Ca2+](in) were not consistent with invasive potential, the changes in pH(in) were, While these conditions decrease the overall amount of gelatinases A and B secreted by these cells, there is a consistent and significant increase in the proportion of the activated form of gelatinase B.
引用
收藏
页码:176 / 186
页数:11
相关论文
共 68 条
[21]   COEXPRESSION OF VIMENTIN AND KERATINS BY HUMAN-MELANOMA TUMOR-CELLS - CORRELATION WITH INVASIVE AND METASTATIC POTENTIAL [J].
HENDRIX, MJC ;
SEFTOR, EA ;
CHU, YW ;
SEFTOR, REB ;
NAGLE, RB ;
MCDANIEL, KM ;
LEONG, SPL ;
YOHEM, KH ;
LEIBOVITZ, AM ;
MEYSKENS, FL ;
CONAWAY, DH ;
WELCH, DR ;
LIOTTA, LA ;
STETLERSTEVENSON, W .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (03) :165-174
[22]   A COMMON SEQUENCE OF CALCIUM AND PH SIGNALS IN THE MITOGENIC STIMULATION OF EUKARYOTIC CELLS [J].
HESKETH, TR ;
MOORE, JP ;
MORRIS, JDH ;
TAYLOR, MV ;
ROGERS, J ;
SMITH, GA ;
METCALFE, JC .
NATURE, 1985, 313 (6002) :481-484
[23]  
ISHIHARA A, 1986, INVAS METAST, V6, P225
[24]  
KATO Y, 1992, J BIOL CHEM, V267, P11424
[25]   ACIDIC EXTRACELLULAR ENVIRONMENT INDUCES ONLY A SUBSET OF HEAT-SHOCK PROTEINS IN PRIMARY MOUSE KIDNEY-CELL-CULTURES [J].
KHANDJIAN, EW .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1990, 68 (04) :804-807
[26]   ISOLATION AND CHARACTERIZATION OF TYPE-IV PROCOLLAGEN, LAMININ, AND HEPARAN-SULFATE PROTEOGLYCAN FROM THE EHS SARCOMA [J].
KLEINMAN, HK ;
MCGARVEY, ML ;
LIOTTA, LA ;
ROBEY, PG ;
TRYGGVASON, K ;
MARTIN, GR .
BIOCHEMISTRY, 1982, 21 (24) :6188-6193
[27]  
KORCZAK B, 1989, CANCER RES, V49, P2597
[28]   CHARACTERIZATION OF AN EXTRACELLULAR MATRIX-DEGRADING PROTEASE DERIVED FROM A HIGHLY METASTATIC TUMOR-CELL LINE [J].
KRAMER, MD ;
ROBINSON, P ;
VLODAVSKY, I ;
BARZ, D ;
FRIBERGER, P ;
FUKS, Z ;
SCHIRRMACHER, V .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1985, 21 (03) :307-316
[29]   STEFINS AND LYSOSOMAL CATHEPSIN-B, CATHEPSIN-L AND CATHEPSIN-D IN HUMAN BREAST-CARCINOMA [J].
LAH, TT ;
KOKALJKUNOVAR, M ;
STRUKELJ, B ;
PUNGERCAR, J ;
BARLICMAGANJA, D ;
DROBNICKOSOROK, M ;
KASTELIC, L ;
BABNIK, J ;
GOLOUH, R ;
TURK, V .
INTERNATIONAL JOURNAL OF CANCER, 1992, 50 (01) :36-44
[30]   THE EFFECTS OF PH AND TEMPERATURE ON FLUORESCENT CALCIUM INDICATORS AS DETERMINED WITH CHELEX-100 AND EDTA BUFFER SYSTEMS [J].
LATTANZIO, FA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (01) :102-108