2-(4-Amino-3-methylphenyl)benzothiazoles are novel compounds with potent and unique
antitumour properties (Shi et al, 1996; Bradshaw et al, 1998a, 1998b; Kashiyama et
al, 1999). It was demonstrated that selective metabolism in vitro of the parent agent
DF 203 (NSC 674495) correlated very highly with its antiproliferative activity, with
uptake and biotransformation observed only in those cell lines that are sensitive
to the compound, such as MCF-7 and T47D breast carcinoma cells (Kashiyama et al, 1999).
CYP1A1, whose expression and activity are induced only in sensitive cells, appears
to be responsible for the metabolic hydroxylation of DF 203 in position 6, which produces
an inactive and antagonistic molecule (Chua et al, 2000). CYP1A1 is also postulated
to have a crucial role in mediating the antitumour activity of DF 203, possibly generating
an electrophilic intermediate responsible for the formation of DNA adducts in sensitive
cells (Stevens et al, 2001).
Fluorinated derivatives of the parent drug DF 203 (see Figure 1
Figure 1
Chemical structures of antitumour 2-(4-amino-3-methylphenyl)benzothiazoles.
for structures) were synthesised in order to prevent deactivation resulting from metabolic
ring hydroxylation (Hutchinson et al, 2001). Fluoro-analogues retain potency and selectivity,
and successfully reduce or abolish the production of inactive and antagonistic metabolites
and the consequent biphasic dose–response phenomenon. Drug-induced induction of CYP1A1,
a crucial event in determining the antitumour specificity of this series of benzothiazoles
(Chua et al, 2000), was not compromised by fluorination (Hutchinson et al, 2001).
2-(4-Amino-3-methylphenyl)-5-fluorobenzothiazole (5F 203, NSC 703786) has emerged
as the most potent of the new generation of antitumour benzothiazoles both in vitro
and in vivo and is currently the focus of pharmaceutical and preclinical development,
as it can be converted to a readily soluble prodrug with appropriate pharmaceutical
properties (Bradshaw et al, 2002).
As for the parent drug DF 203, depletion of 5F 203 from culture media and subsequent
induction of CYP1A1 correlate with cell responsiveness. Only in sensitive cells does
drug uptake occur and CYP1A1 enzyme expression increase to detectable levels; naturally
occurring drug-resistant cells do not show significant changes in either drug levels
in medium or CYP1A1 expression (Brantley et al, 2001).
We have previously reported that the parent compound DF 203 induces activation of
the AhR in sensitive cells such as human breast epithelial cancer MCF-7 cells. In
contrast, nonresponsive cells, for example, breast carcinoma MDA-MB-435 or prostate
carcinoma PC-3 cells, showed no activation of the AhR and no induction of CYP1A1 after
drug treatment (Loaiza-Pérez et al, 2002). We also have reported a suitable model
to investigate the role of the AhR in mediating drug cytotoxicity (Loaiza-Pérez et
al, 2001), consisting of AhR-deficient AHR100 cells, derived from MCF-7 human breast
epithelial cancer cells by continuous exposure to escalating concentrations of benzo[a]pyrene
(Yeh et al, 2001). AHR100 cells display relative resistance to the cytotoxic effects
of several polycyclic aromatic hydrocarbons (PAHs), such as benzo[a]pyrene and dimethylbenz[a]anthracene
(DMBA), due to impairment of the AhR signal transduction pathway (Yeh et al, 2001;
Ciolino et al, 2002).
We therefore have used wild-type MCF-7 and AHR100 cells as a model, to investigate
the molecular determinants for sensitivity to the clinical candidate 5F 203, including
toxicity, cell cycle distribution, DNA damage, CYP1A1 activity and AhR signalling
pathway activation. The results presented in this paper confirm that activation of
the AhR plays an essential role in 5F 203 antitumour activity, mediating responsiveness
and efficacy.
MATERIALS AND METHODS
Drug and cell culture
5F 203 was synthesised by the Cancer Research Laboratories at the University of Nottingham,
UK and the Drug Synthesis and Chemistry Branch, NCI, following published methods (Hutchinson
et al, 2001). The compound was dissolved in DMSO to make a 100 mM stock concentration
and further diluted to the working concentration (1 nM–100 μ
M) for experimental procedures. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) was prepared
as 10 μ
M top stock dissolved in DMSO and diluted to the working concentration (10 nM) immediately
prior to use. MCF-7 cells were obtained from the National Cancer Institute Repository
(National Cancer Institute-Frederick Cancer Research and Development Center, Frederick,
MD, USA) and grown in RPMI 1640 medium supplemented with 10% fetal bovine serum (FBS)
(Invitrogen, Carlsbad, CA, USA). AhR-deficient AHR100 cells were generated from wild-type
MCF-7 cells by 6–9-month exposure to benzo[a]pyrene and subsequently demonstrated
a 100-fold higher resistance to benzo[a]pyrene than the wild-type line. Additional
characterisation indicated that AHR100 cells contained reduced amounts of AhR and
normal levels of the aryl hydrocarbon receptor nuclear translocator (ARNT) (Ciolino
et al, 2002).
Assessment of cytotoxicity
Cells were inoculated in 96-well plates and maintained for 24 h before treatment with
5F 203, which consisted of five serial dilutions (1 : 10) ranging from 10 nM to 100 μ
M. Treated cells were subsequently maintained for an additional 48 h, and cellular
protein was measured by the sulphforhodamine-B (SRB) assay as described previously
(Monks et al, 1991). Briefly, cells were fixed with trichloroacetic acid and stained
with SRB. Protein-bound SRB was solubilised and measured spectrophotometrically to
determine relative cell viability in treated and untreated cells.
4,6-Diamidino-2-phenylindole (DAPI) staining
Approximately 2×105 cells were grown on coverslips overnight. Cells were exposed to
DMSO (0.1%) or 5F 203 (1 μ
M) for 24 h. Floating cells contained in the supernatant were collected by cytocentrifugation,
and stained with 0.4% DAPI. Experiments were repeated at least three times. Stained
cells were then visualised on a Zeiss Axiovert microscope using ×63 objective and
images were captured with an Optronics CCD camera (Loaiza-Pérez et al, 2002).
32P-postlabelling assay
Pellets of control and treated (0.1% DMSO or 1 μ
M 5F 203 for 24 h) MCF-7 and AHR100 cells were used for DNA extraction using Qiagen
DNA extraction columns according to the manufacturer's protocol. Of each extracted
DNA 5 μg was digested to deoxynucleoside 3′-monophosphates by incubating with micrococcal
nuclease (175 mU) and calf-spleen phosphodiesterase (6 mU) at 37°C overnight. DNA
adduct enrichment was carried out by butanol extraction (Gupta, 1985). Adducts were
then radiolabelled by 5′-phosphorylation using 62.5 μCi of [γ-32P]ATP and 5 U of T4
polynucleotide kinase.
HPLC detection and quantification of DNA adducts
32P-labelled products were separated on a Hypersil BDS C18 analytical column (250×4.6 mm,
5 μm; Shandon). The mobile phase consisted of 88% 2 M ammonium formate (pH 4.0) and
12% acetonitrile for 50 min, followed by a linear gradient of 20–45% acetonitrile
for 15 min. Radioactivity was monitored by a radiochemical detector (Lab Logic, β-RAM)
lined to a Varian Star 9012 pump. Data analysis was done by Laura, an MS Windows package
(Lab Logic Inc.). The relative adduct levels (RAL) were calculated by the method of
Reddy and Randerath (1986), based on the specific activity of [γ-32P]ATP and the amount
of DNA used. RAL values were then translated into fmol adducts per μg DNA (Gupta,
1985).
Cell cycle analysis
Cell cycle analysis on MCF-7 and AHR100 cells was performed as described previously
(Sherwood and Schimke, 1995). Briefly, exponentially growing cells were exposed to
either DMSO (0.1%) or 5F 203 (1 μ
M) for 24 h, then harvested, washed briefly, in cold PBS and fixed in 70% ethanol.
DNA was stained by incubating the cells in PBS, containing propidium iodide (50 μg ml−1)
and RNAase A (1 mg ml−1) for 30 min at 37°C and fluorescence was measured and analysed
using FACSCaliber (Becton Dickinson Immunocytometry Systems, San José, CA, USA) and
ModFit (Verity Software, Topsham, ME, USA).
CYP1A1 activity in intact MCF-7 and AHR100 cells
MCF-7 and AHR100 cells were grown in 24-well plates to 60–70% confluence prior to
treatment with 0.1% DMSO (control) or 5F 203 (1 nM–1 μ
M). At the end of the incubation period, the medium was aspirated and the cells were
washed with PBS. CYP1A1 enzyme activity was subsequently determined by 7-ethoxyresorufin-O-deethylase
(EROD) activity in intact cells as described by Kennedy and Jones (1994). Briefly,
the fluorescence of resorufin generated from the conversion of ethoxyresorufin by
CYP1A1 was measured spectrophotometrically and resorufin content was derived from
a standard curve.
Real-time RT–PCR
Evaluation of CYP1A1 and CYP1B1 gene expression in MCF-7 and AHR100 cells was performed
by real-time RT–PCR, using 15 cycles of PCR, primers and probes described in a previous
report (Loaiza-Pérez et al, 2002). RNA was isolated using Qiagen kits (Qiagen, Valencia,
CA, USA). PCR efficiencies were validated by means of a standard curve.
Transfections
Cells were transfected using LipofectAMINE (Invitrogen), with 0.5 μg Renilla reniformis
luciferase (pRL-TK) (Promega, Madison, WI, USA), and 1.5 μg of pTX.Dir or pT81 as
described previously (Loaiza-Pérez et al, 2002). Luciferase activity was measured
by the Dual-Luciferase Assay System (Promega, Madison, WI, USA) following the manufacturer's
instructions, and transfection efficiency was monitored by the activity of the R.
reniformis plasmid.
Electrophoretic mobility shift assay (EMSA)
Synthetic oligonucleotides containing the AhR-binding site of the human CYP1A1 promoter
(5′-CTC CGG TCC TTC TCA CGC AAC GCC TGG GCA-3′) (Invitrogen) were used as probes.
Electrophoretic mobility shift assays were performed as described previously (Loaiza-Pérez
et al, 2002). Briefly, nuclear extracts (20 μg) from control (0.1% DMSO) and treated
(1 μ
M 5F 203 for 1 h, or 10 nM TCDD for 1 h) MCF-7 and AHR100 cells were incubated in
binding buffer with the [32P]DNA probe and the resulting DNA/protein DNA complexes
were separated on a 6% polyacrylamide gel (Novex) under nondenaturing conditions and
high ionic strength. Gels were dried and imaged by autoradiography.
RESULTS
5F 203-induced cytotoxicity correlates with AhR activation in sensitive MCF-7 cells
Previous observations have shown that cytotoxicity of benzothiazoles is mediated via
activation of the AhR signalling pathway (Kashiyama et al, 1999; Chua et al, 2000;
Loaiza-Pérez et al, 2002). In addition, cytotoxicity across a large panel of human
tumour cell lines correlates with CYP1A1 inducibility (Hose et al, 2001). We then
sought to investigate responsiveness of MCF-7 wild-type cells to the clinical candidate
5F 203 as compared to that of MCF-7-derived AhR-deficient cells (AHR100). Specifically,
we sought to establish whether AhR-mediated signalling could account for all the cytotoxic
potential of this agent. Figure 2A
Figure 2
(A) Selective cytotoxicity of 5F 203 to MCF-7 cells. Growth inhibition induced by
5F 203 was assessed by sulphforhodamine B assay as detailed in Materials and Methods.
Values are means±s.d. (n=10). (B) 5F 203 induces changes in nuclear morphology of
5F 203-sensitive MCF-7 breast cells but not AHR100 cells. Cells prepared as described
in Materials and Methods were exposed for 24 h to 0.1% DMSO (control) or 1 μ
M 5F 203, and stained with 4,6-diamidino-2-phenylindole (DAPI).
indicates that MCF-7 cells are sensitive to this compound (GI50=121 nM, 48 h exposure).
In contrast, AHR100 cells show a decreased growth inhibition after treatment with
high drug concentration (GI50>100 μ
M) and can therefore be considered resistant.
As a complementary approach, MCF-7 and AHR100 cells treated with 0.1% DMSO (control)
or 5F 203 (1 μ
M) for 1 h were subsequently stained by DAPI (Figure 2B). Only MCF-7 cells treated
with the drug showed altered nuclear morphology, which included chromatin condensation
and marginalisation to the nuclear membrane. AHR100 cells failed to show any significant
morphological changes. Taken together, Figure 2A and 2B suggests that activation of
the AhR signalling pathway participates in the antiproliferative activity of 5F 203,
which results in growth inhibition and modified nuclear features.
5F 203 induces DNA adduct formation in MCF-7 cells
We next questioned whether DNA adducts could be produced in MCF-7 and AhR-deficient
AHR100 cells. DMSO-treated MCF-7 and AHR100 cells showed a similar profile of DNA
adducts, with a few adducts eluting within the early retention time (⩽20 min) (Figure
3
Figure 3
DNA adduct profiles in (A) MCF-7 and (B) AHR100 cells. Cells were incubated with (i)
0.1% DMSO or (ii) 1 μ
M 5F 203 for 24 h. 32P-labelled adducts were analysed using 2 μg digested DNA on a
Hypersil C18 column with a gradient of acetonitrile in 2 M ammonium formate as detailed
in Materials and Methods. The early peak is due to the presence of free [γ-32P]ATP.
). After treatment with 1 μ
M 5F 203, no significant changes in these peaks were found in either cell lines, while
several other adducts with longer retention time were detected. The major adduct formed
in AHR100 cells (adduct 17 in Figure 3Bii) is chromatographically equivalent to an
adduct detected in MCF-7 cells (adduct 7 in Figure 3Aii). Although DNA adduct profiles
appear similar in the two cell lines, the number of total adducts/108 nucleotides
induced by drug treatment was greatly decreased in AHR100 cells compared to wild-type
MCF-7 cells. These findings suggest that impairment of the AhR signalling pathway
may result in reduced activation of 5F 203 into reactive species able to damage DNA.
5F 203 causes altered cell cycle distribution
As our results in Figure 2 and Figure 3 indicated that 5F 203 was inducing the formation
of DNA adducts, we investigated whether this could result in an altered cell cycle
profile. For this approach, cells sensitive (MCF-7) and insensitive (AHR100) to 5F
203 were exposed to 1 μ
M of the drug or 0.1% DMSO for 24 h and subsequently processed for cell cycle analysis.
As illustrated in Figure 4
Figure 4
5F 203 induces accumulation of cells in S phase. Exponentially growing cells (MCF-7
and AHR100) were exposed to either 0.1% DMSO (control) or 5F 203 (1 μ
M) for 24 h, harvested, washed in PBS, and fixed in 70% ethanol. DNA was stained by
incubating the cells in PBS containing propidium iodide and fluorescence measured
and analysed as described in Materials and Methods.
, 5F 203 treatment of MCF-7 cells caused a notable increase in G1 (37 to 52%) and
S (20 to 27%) phase cells, which coincided with a decrease in G2/M (42 to 16%) phase
cells. Accumulation of cells in sub-G1 was minimal when compared to control. In contrast,
5F 203-insensitive cells (AHR100) failed to demonstrate any notable effect on the
cell cycle, in particular S, G2/M and sub-G1 phases. The data demonstrate that 5F
203-induced DNA damage may lead to cell accumulation in G1 and S phase concomitant
with growth inhibition. As MCF-7 cells are p53 wild type, their response to 5F 203
treatment is consistent with the operation of a G1- and possibly S-phase checkpoint
to cell cycle progression after DNA adduct formation.
CYP1A1 and CYP1B1 induction
5F 203 induces DNA damage and cell cycle arrest most obviously in MCF-7 cells with
a fully functional AhR signalling pathway. The hypothesis that deficient activation
of CYP1A1 might occur in AhR-deficient AHR100 cells was then addressed. The enzymatic
activity of CYP1A1 in intact MCF-7 and AHR100 cells treated with 5F 203 was assayed
by measuring EROD activity. Although both CYP1A1 and CYP1B1 can catalyse the dealkylation
of ethoxyresorufin, the specific activity of CYP1A1 is approximately 40-fold higher
than that of CYP1B1 (Doostdar et al, 2000). Incubation with 5F 203 for 24 h resulted
in a concentration-dependent increase in EROD activity over a range of 50 nM to 1 μ
M in MCF-7 cells, whereas the drug had no effect on EROD activity in AHR100 cells
(Figure 5A
Figure 5
(A) 5F 203 induces CYP1A1 activity in MCF-7 but not in AHR100 cells. MCF-7 and AHR100
cells were incubated for 24 h with DMSO (0.1%) and 5F 203 (1 μ
M) for 24 h and assayed for CYP1A1 enzyme activity by EROD assay as described in Materials
and Methods. n=4±s.d. (B) 5F 203 induces CYP1A1 and CYP1B1 mRNA levels in sensitive
(MCF-7) cells. MCF-7 and AHR100 cells were treated with 5F 203 (1 μ
M) for 24 h, RNA was isolated from control and treated samples and CYP1A1 and CYP1B1
gene expression were measured by real-time RT–PCR as described in Materials and Methods.
Data are shown as fold induction of treated cells relative to constitutive expression
in control cells (±s.d., n=7 samples from two independent experiments).
).
In order to compare the effect of 5F 203 on CYP1A1 and CYP1B1 gene expression, MCF-7
and AHR100 cells were treated with the compound (1 μ
M) for 24 h and mRNA levels for these two genes were measured by real-time RT–PCR.
5F 203 caused an increase in the mRNA levels of both cytochromes in MCF-7 cells, where
relative levels of CYP1A1 mRNA were approximately 100-fold higher when compared to
control; only a minimal increase of CYP1B1 mRNA (10-fold) was observed (Figure 5B).
In contrast, in AHR100 cells, levels of CYP1A1 and CYP1B1 mRNA after treatment remained
similar to control (Figure 5B). These findings are in agreement with previous studies
which described that the parent compound DF 203 causes induction of CYP1A1 protein
and increase in mRNA levels in MCF-7 cells but not in DF 203 inherently resistant
cells (Chua et al, 2000; Loaiza-Pérez et al, 2002).
5F 203 increases protein/DNA complex formation on the XRE sequence of CYP1A1 in MCF-7
but not AHR100 cells
CYP1A1 and CYP1B1 promoters are regulated by the AhR, which forms a heterodimer with
ARNT. Binding of the complete dimer to the XREs in the promoter region mediates transcription
of AhR-responsive genes, including CYP1A1 and CYP1B1 (Whitlock, 1999). MCF-7 and AHR100
cells were transfected with an XRE-luciferase reporter construct (pTX.Dir); as control,
the same reporter construct but without the XRE (pT81) was used. Cells were then treated
with DMSO (0.1%), TCDD (10 nM) or 5F 203 (1 μ
M). TCDD was used as a prototypic compound activator of CYP1A1 transcription and included
as a positive control. As shown in Figure 6A
Figure 6
(A) 5F 203 induces binding to the XRE sequence of CYP1A1. MCF-7 and AHR100 cells were
transfected with XRE-luciferase (pTX.Dir.) or pT81. A schematic of the respective
construct is shown below the panel. Transfected cells were treated with DMSO, TCDD
(10 nM) or 5F 203 (1 μ
M) for 9 h. XRE-luciferase activity was determined normalizing to the amount of Renilla
reniformis luciferase. The values are expressed as luciferase levels relative to control.
(B) 5F 203 induces protein/DNA complexes on the XRE sequence of the CYP1A1 promoter.
Nuclear extracts (20 μg) prepared from MCF-7 cells treated with 0.1% DMSO (C) (lane
1), TCDD (10 nM, 1 h) (lane 2) or 5F 203 (1 μ
M, 1 h) (lane 3) were incubated with labelled XRE sequence derived from the CYP1A1
promoter for 10 min at room temperature. Free and bound DNA were separated as described
in Materials and Methods. In competition experiments, nuclear extracts from MCF-7
cells treated with 5F 203 (1 μ
M, 1 h) were incubated with 4 μg of anti-AhR antibody (lane 6), 100-fold excess of
unlabelled XRE oligonucleotide (lane 7), 100-fold excess of unlabelled Sp1 oligonucleotide
(lane 8) or 4 μg of IgG antiserum (lane 9). Protein/DNA complexes from AHR100 cells
were resolved in the same gel. Nuclear extracts from these cells (20 μg) treated with
DMSO (lane 4) or 5F 203 (1 μ
M, 1 h) (lane 5) were incubated with radioactive XRE and resolved by the same procedure.
, in MCF-7 cells transfected with pTX.Dir, a 15-fold induction of luciferase activity
was observed with TCDD, and 5F 203 treatment similarly resulted in a 15-fold induction.
However, when AHR100 cells were transfected with XRE and treated with 5F 203 (1 μ
M), XRE-luciferase activity was demonstrated to be only approximately 1.7-fold higher
than control. No induction in luciferase activity was observed when cells transfected
with pT81 were treated with 5F 203 (1 μ
M) or TCDD (10 nM). Similar results were obtained when cells were transfected with
a fragment of mouse native CYP1A1 promoter (inclusive of four dioxin responsive elements
(DREs)) (pGudLuc1.1) (data not shown) (Garrison et al, 1996). When pTX.Dir-transfected
cells were pretreated with an antagonist of AhR, α-naphthoflavone, before treatment
with 5F 203, luciferase activity was reduced approximately 25%, suggesting competition
between the two ligands for binding to the AhR (results not shown).
In order to compare protein/DNA complex formation on the XRE of CYP1A1 promoter after
treatment with 5F 203 in MCF-7 and AHR100 cells, electrophoretic mobility shift assays
were performed. Previous reports from our laboratory (Loaiza-Pérez et al, 2002) described
that, in MCF-7 cells, three protein/DNA complexes were found in nuclear extracts of
control cells, although the intensity of the uppermost complex was lower than the
others (Figure 6B, lane 1). 5F 203 (1 μ
M) treatment for 1 h (lane 3) caused a 15-fold induction of the binding of the uppermost
complex. This induction exceeded that afforded by TCDD (10 nM, 1 h) treatment (lane
2). AHR100 cells exposed for 1 h to 5F 203 (1 μ
M) showed considerable attenuation of induction (lane 5). When nuclear extracts from
cells treated with 5F 203 (1 μ
M) for 1 h were pretreated with AhR polyclonal antibody (lane 6) or 100× unlabelled
XRE probe (lane 7), the binding of the three complexes to labelled XRE sequences was
greatly diminished. These protein/DNA complexes did not disappear when nuclear extracts
from 5F 203-treated cells were preincubated with 100× unlabelled SP1 oligonucleotide
(lane 8) or IgG antiserum (lane 9).
DISCUSSION
We report here that treatment with 5F 203 causes accumulation in the G1 and S phase,
along with growth inhibition in wild-type MCF-7 cells, but it does not affect cell
cycle progression of AHR100 cells. We also confirm the production of DNA damage in
these sensitive cells (Stevens et al, 2001), whereas the formation of DNA adducts
is significantly reduced in the resistant subclone (Figure 3). These results corroborate
the view that antitumour activity of 5F 203 is highly dependent on functional AhR
signalling, whose impairment results in reduced efficacy of the agent.
Activation of the AhR signalling pathway may be an important factor determining sensitivity
to 5F 203 because it triggers metabolic transformation of the drug through CYP1A1
into reactive species damaging DNA. Our data show that exposure of AHR100 cells to
5F 203 produces markedly fewer DNA adducts, as compared to wild-type MCF-7 cells.
The chemical structure of these adducts has not yet been characterised. Computational
studies using frontier molecular orbital calculations point to the putative reactive
species being a nitrenium ion (Dr SE O'Brien, personal communication), but further
studies are required to confirm this hypothesis and identify the adducts. A more detailed
description of the formation of DNA adducts induced by benzothiazoles in sensitive
cells will be published separately.
MCF-7 cells have proven to be a valuable and extensively used model for studies involving
the AhR and CYP1A1 expression (Dohr et al, 1995; Wang et al, 1995; Jorgensen and Autrup,
1996). Experiments reported elsewhere (Yeh et al, 2001) have demonstrated that resistance
to aryl hydrocarbons in AHR100 cells is a consequence of decreased expression of the
AhR, which results in impaired induction of CYP1A1 and probably represents an adaptation
to long-term culture with polycyclic aromatic hydrocarbons (PAHs). This leads to a
diminished capacity to activate PAHs like DMBA, thereby decreasing the level of apoptosis
caused by exposure to PAHs. Apoptosis induced by DMBA could be blocked by inhibitors
of DMBA metabolism such as α-naphthoflavone and diosmetin. These data demonstrated
that PAH resistance in these cells is mediated by changes in the signal transduction
pathway which regulates CYP1A1 expression (Ciolino et al, 2002). Previous reports
have demonstrated that the growth-inhibitory properties of the parent compound, DF
203, were abrogated when MCF-7 cells were cotreated with an AhR antagonist like α-naphthoflavone
(Chua et al, 2000). These findings suggested that activation of AhR mediates sensitivity
of MCF-7 cells to benzothiazoles. The fact that adriamycin-resistant MCF-7 cells (NCI/ADR-RES
cells), which are also deficient in AhR signalling (Caruso and Batist, 1999), are
resistant to benzothiazoles (Chua et al, 2000) further supports this hypothesis.
Activation of phase I enzymes, such as CYP1A1 and CYP1B1, usually occurs as a response
to promote detoxification of xenobiotics; however, metabolic enzymes may convert inert
compounds into potentially harmful products. This is the case for most PAHs, including
benzo[a]pyrene, which induces CYP1A1 via the AhR signalling pathway and is metabolised
into reactive species that cause DNA damage (Szeliga and Dipple, 1998; Burczynski
and Penning, 2000) resulting in G1 cell cycle arrest (Vaziri and Faller, 1997). In
contrast, the environmental pollutant TCDD, which is the most potent AhR agonist,
induces CYP1A1 and modulates CYP1B1 expression in MCF-7 cells (Dohr et al, 1995),
but is not directly genotoxic. It has been hypothesised that TCDD-induced alterations
in estrogen metabolism may lead to increased generation of reactive oxygen species
and consequent induction of DNA adducts (Wyde et al, 2001).
In addition to selective metabolism, differential modulation of AhR functions could
underlie specific cytotoxicity of the agent. Activation of the AhR signalling pathway
consists of several steps, including translocation, pairing with nuclear factors,
transactivation of gene transcription and degradation (Rowlands and Gustaffson, 1997),
each of which might be differentially regulated in different cells. Other proteins,
which integrate the function of the AhR, like heat-shock protein 90 or ARNT, may also
be related to differential sensitivity to 5F 203. For example, Qin et al (2001) have
demonstrated in patients that there is an association of ARNT splice variants with
ER-negative breast cancer, poor induction of vascular endothelial growth factor under
hypoxia, and poor prognosis. Further studies are necessary to determine, in greater
detail, aspects of the pathway that may be altered in 5F 203-sensitive cells.