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Anthracyclines
Anthracyclines are anticancer compounds that were originally derived fromStreptomycesand their
anti-tumor activities were established in the 1960s[1]. Anthracyclines are red aromatic polyketidesand occur in variety of forms due to the structural differences in the aglycone and the different
sugar residues attached[2].
Major Drugs in the class
Daunorubicin
Daunomycin (daunorubicin) was the first anthracycline compound to be chatacterized structurally
and stereochemically. Danorubicin is used in treating acute lymphoblastic and myeloblastic
leukaemias.
Doxorubicin
Adriamycin (generic name doxorubicin) is a hydroxyl derivative of daunorubicin is [3, 4].
Doxorubicin is one of the most widely used chemotherapeutic agents and is generally prescribed incombination with other drugs.Doxorubicin has a broad spectrum of activity. It is one of the most
effective drugs for solid tumor treatment, e.g., breast cancer, small cell lung cancer and ovarian
carcinoma treatments. It has significant activity against bladder, stomach, liver and thyroid tumors,Ewings and osteogenic bone tumors, soft tissue sarcoma, neuroblastoma and Wilms tumor. It is also
active against multiple myeloma, several types of leukaemia and cutaeneous T-cell lymphoma. It is
also plays an important role in treatment of Hodgkins disease and non-Hodgkins lymphomas[5].
Due to development of resistance in the tumor cells to daunorubicin and doxorubicin, dose
dependent cardiotoxicity, and several other side-effects, modification of these drugs to produce
analogs with wider activity and lower toxicity have been sought. Efforts to find better
anthracyclines and over the years the number of analogs have risen to more than 2000 [6]. However,
only very few anthracycline analogs like epirubicin and idarubicin[7] have been approved for clinical
use.
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Epirubicin
Epirubicin is an epimer of doxorubicin and differs only in the orientation of the C-4 hydroxyl group
on the sugar. Because of this slight change in the structure, epirubicin has lower cardiotoxicity thandoxorubicin. Epirubicin is used in the treatment of gastric and breast cancer and is also indicated
for the treatment of carcinoid, endometrial, lung, ovarian, esophageal and prostate cancers as well
as soft tissue sarcomas [5].
Idarubicin
Idarubicin is an analog of daunorubicin. It lacks the C-4 methoxy group and this increases its
lipophilicity. Idarubicin has improved activity as induction therapy for acute myelogenous
leukaemia[5].
Valrubicin
Valrubicin is N-trifluoroacetyl, 1-4-valerate derivative of doxorubicin. Valrubicins enters cells more
rapidly than doxorubicin. It is used specifically in the treatment of early bladder cancer [8].
Mechanism of action
The mechanism by which anthracyclines inhibit cancer is still not completely clear and multiple
pathways are thought to be involved in the cytotoxicity of this class of anti-cancer drugs. The useful
pathways are the ones that are actually involved in toxicity to the neoplasia while not being toxic to
the organism.
Accumulation of anthracyclines in the nucleus of neoplastic and proliferating cells
Anthracyclines enter the cells through passive diffusion[9]. An elegant mechanism of the selective
transport of anthracyclines to the nuclei of neoplastic and proliferating cells has been proposed by
Kiyomiya and colleagues[10, 11]. It has been demonstrated with doxorubicin that once it enters the
cells, it binds the proteasomes in the cytoplasm for which it has high affinity. The drug-proteasome
complex is then translocated into the nucleus. Proteasomes are shown to be located predominantly
in the nucleus of neoplastic and normal proliferative cells as compared to the non-proliferative
normal cells that show the presence of proteasomes predominantly in the cytoplasm[12-14]. Thus
there will be a relatively higher transport of anthracyclines into the nucleus of the neoplastic and
non-differentiated, proliferative normal cells. Once the anthracyclines reach the nucleus they would
dissociate from the proteasome and bind DNA due to its higher affinity for DNA. This would bringabout the DNA mediated effects of anthracyclines. Moreover, binding of anthracyclines to
proteasomes also inhibits the protease activity leading to inhibition of degradation of proteins
involved in cell growth and metabolism and thus inducing apoptosis of these cells.
DNA intercalation
Intercalation into DNA leading to inhibition of macromolecular synthesis was the first mechanism
described for cytotoxicity of anthracyclines[15]. The rather strong binding of daunorubicin and
doxorubicin to DNA has been characterized extensively [16-18]. However, it has been seen with other
anthracyclines like those of the nogalamycin family that the antitumor activity correlates with a
decrease in affinity for DNA [19, 20]. Considering this and also taking into account that the DNA in
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cells does not occur naked but as chromatin, it seems unlikely that DNA intercalation is the only or
most essential pathway of anthracycline cytotoxicity.
On the other hand, anthracyclines like doxorubicin at low concentrations have been shown toselectively displace nuclear proteins[21], and daunorubicin has been shown to induce aggregation of
chromatin[22]. The proposed mechanism involves initial intercalation of the drug into the linker
regions where the DNA is free of nuclear proteins, leading to conformational changes in DNA that
extend towards the histone octamer and result in the unfolding of chromatin and its subsequent
aggregation[22].
Interaction with DNA binding proteins
Regulation of gene expression by inhibiting, or promoting, the binding of transcription factors is
also considered to play a role in anthracycline cytotoxicity with the potential involvement of SP-1
transcription factor as a specific target for these drugs [23, 24]. Involvement of anthracyclines in
inhibiting DNA synthesis by affecting the initiation or the elongation phase, and RNA synthesis by
inhibiting RNA polymerase activity has also been documented[25-27]. Another mechanism that hasgained ground is the anthracycline activity as Topoisomerase II poisons[28]. After DNA intercalation,
anthracycline rings that do not intercalate into the DNA seem to play a role in stabilizing the
complex between Topoisomerase II and the DNA that it has nicked. The DNA nicks cannot be sealed
and this leads to an accumulation of DNA damage that is cytotoxic due to growth arrest in G1 and
G2 and programmed cell death[29]. Doxorubicin and Idarubicin have also been showed to inhibit
Topoisomerase I and this is proposed to be an ancillary mechanism of cytotoxic activity of
anthracyclines[30].
Anthracyclines, p53 and apoptosis
Like any other genotoxic agent, doxorubicin has been demonstrated to induce the binding of p53 to
DNA. As p53 is a major player in some forms of apoptosis, it has been proposed that anthracyclines
may exert their cytotoxic effect via p53 mediated apoptosis. There are contradictory reports
regarding this link between anthracyclines, p53 and apoptosis[29, 31, 32]. It is observed that there are
more DNA breaks in p53 proficient cells than in p53 deficient cells although the levels ofTopoisomerase II are same in the two cell types. It is therefore also proposed that p53 exerts this
activity by binding to Topoisomerase II and inhibiting its ligase activity [33, 34]. However, clinical
concentrations of these drugs induce apoptosis pathways that do not always require p53 by
triggering a cyclic cascade of sphingomyelin hydrolysis and formation of ceramide [35]. It is also
observed that anthracyclines can release cytochrome C from mitochondria directly and induce
apoptosis[36]. Thus, although p53 seems to play some role in the activity of anthracyclines, it is not
necessarily the only mechanism.
Free radical generation
One electron addition to the quinone moiety in ring C of anthracyclines leads to formation of
semiquinone that regenerates back to quinone by reducing oxygen to reactive oxygen species like
superoxide anion and hydrogen peroxide. The semiquinone can oxidize with the bond between ring
A and daunosamine which results in deglycosylation. The aglycone thus formed has higher
solubility in lipids and can intercalate into biological membranes and form reactive oxygen species
which can affect sensitive targets[37, 38]. The one electron redox cycle of doxorubicin has beendemonstrated to induce the release of iron from the stores. Doxorubicin forms complex with iron
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and this complex is capable of producing hydroxyl ions which is a more potent reactive oxygen
species[39, 40]. Thus, there seems to be involvement of oxidative damage in the mechanism of
anthracycline activity. However, as the production of measurable reactive oxygen species is
predominantly observed at supraclinical concentrations, this may not be the direct mechanism ofanthracycline activity. Reactive oxygen species though can act as signaling molecules at very low,
unmeasurable concentrations and induce apoptosis and this could be one of the mechanism by
which anthracyclines exert their cytotoxic effect.
Antiangiogenic mechanism
A recent study[ shows that the anthracyclines inhibit transcriptional factor HIF-1 from binding to
DNA in hypoxic human cells and inhibited tumor growth in human prostate cancer xenografts.
Inhibition of HIF-1 transcriptional activity leads to decreased VEGF, SDF1 and SCF expression
because of which there is decreased CAC mobilization and this results in decreased tumor
vascularization and growth. Thus, anthracyclines can also inhibit cell growth through
antiangiogenic pathways.
Side Effects
The side effects of anthracyclines, like any other chemotherapeutic agent, are linked to their
cytotoxicity to non-differentiated, proliferating normal cells. These side effects include nausea,
vomiting, and alopecia. However, the major toxicities of anthracyclines include cardiotoxicity and
myelosuppression and these are the major limitations of these drugs. Doxorubicin can also causesevere local tissue necrosis. Cardiomyopathy and congestive heart failure are the two cardiotoxic
side effects of anthracyclines. Epirubicin is less cardiotoxic than doxorubicin but may not totally
eliminate the risk of chronic cardiotoxicity[5].
Anthracycline induced cardiotoxicity is irreversible and is thus an especially important
consideration in treatment of curative malignancies in pediatric patients[4. As discussed in the
mechanism of action of anthracyclines, the interaction between anthracyclines and iron[ is found to
play a role in anthracycline induced cardiomyopathies by producing potent reactive oxygen species.
An iron chelator dexrazoxane has now been approved for use in patients who are prescribed high
doses of doxorubicin to prevent cardiotoxicity.
Various other strategies to prevent the cardiotoxicity of anthracyclines are also being employed
that include change in administration of the drugs, limiting the overall dosage, encapsulation into
liposomes, combination treatment, use of cardioprotectors and synthesis of modified
anthracyclines[5].
Allergic reactions
Although rare, mild to medium allergic reactions have been reported for anthracyclines. The
symptoms include generalized urticaral exanthema as reported for epirubicin and doxorubicin.High doses of epirubicin can cause high fever, hypertension and hypoxia as hypersensitivity
symptoms. Pegylated and liposomal doxorubicine and daunorubicin that have lower toxicity have
been reported to produce acute hypersensitivity infusion reactions.