Cancer chemotherapy resistance is the primary cause that leads
to an ineffective chemotherapeutic response in patients. The emergence of chemotherapy
resistance can be seen before starting chemotherapy (primary, innate or
intrinsic resistance), or in the course of chemotherapy (Aquired or extrinsic resistance)
1,2,7. Also, chemotherapy failure can arise from factors related to the host 1.
However, researchers focus on figuring out factors related to the tumor that
elicit chemotherapy failure or resistance 1. For example, treatment of Hepatocelular
carcinoma (HCC), multiple myeloma, and breast cancer is difficult due to genetic
or epigenetic changes in cancer cells leading to marked chemotherapy resistance
4,6,7. Resistance mechanisms are abundant and complex 2. The major
mechanism that elicits chemotherapy resistance is the expression of ATP-binding cassette (ABC)
transporters in a great amount, and that can increase efflux of drugs from cancer
cells, thereby decrease the concentration of the drug inside the cell 3.
Chemotherapy resistance can be divided into three divisions: (1) Macroscopic
(systemic) resistance host–related factors, (2) Microscopic (local) resistance
tumor related factors and (3) Mesoscopic (physical, mechanical) or (regional)
resistance tumor—host interacting factors 1.
Macroscopic (systemic) resistance host–related factors
For an effective chemotherapy, a chemotherapeutic agent must
reach the tumor 1. Therefore, the pharmacokinetics are an important
host-related factors which have an influence in the chemotherapeutic efficacy
1. If the drug doesn’t reach its target in a sufficient level, we call this
Oral administration of the chemotherapeutic agent is better
than intravenous administration, because: (1) There is no hospitalization
required, (2) it prolongs it’s time for clearance, which increase antitumor
activity, (3) it decrease drug toxicity, (4) it enhance patient compliance 1.
However, to maintain a sufficient amount of orally administered chemotherapeutic,
several factors should be taken into consideration 1:
1. P-gp (Permeability glycoprotein)
P-gp is located in the gastrointestinal tract, including the
small intestine where absorption of most anticancer drugs takes place 1. P-gp
overexpression can occur due to genetic polymorphism, pathological condition
and concomitant administration of some anticancer drugs 1. This result in
decreased bioavailability of antineoplastic agent 1.
Food can affect absorption and bioavailability of
antineoplastic agent 1. For example, a high-fat meal decreases the rate of
absorption of Topotecan, but it does affect its extent of absorption 1. St
John’s wort, reduces the efficacy of some antineoplastic agent by inducing the
expression of Pregnane X receptor, a xenobiotic or detoxification sensor 1.
Grapefruit juice, decrease the metabolism of antineoplastic agent in the
intestine by reducing the presence of CYP3A4, a metabolizing enzyme 1.
The distribution of the drug between plasma and tissues
depends on several factors 1. Some of them include:
For example, metronidazole has a low volume of distribution
in women 1.
Dose adjustment is needed in cancer patients as they lose
weight because of tumor progression 1.
3. Plasma Proteins
Changes in the plasma concentration of albumin or
Alpha-1-acid glycoprotein result in variable anticancer activity due to binding
of some anticancer agents to these proteins 1.
The best time for administration of anticancer agent is at
night, because the basal metabolic rate is increased at night. This result in
increase activity of anticancer agents since they act against highly
proliferating cells, mainly cancer cells 1.
Drug metabolism is different from anabolism and catabolism
1. Its main role is detoxification or activation of drugs 1.
CYP450 (Cytochrome P450) Enzymes, can activate some
antineoplastic agent, as well as inactivate them 1. Overexpression of CYP450
in cancer patients might lead to resistance due to the rapid inactivation of
antineoplastic agent 1.
GSTs (Glutathione–S–Transferases), overexpression of
GSTs in cancer patients might lead to resistance 1. It is involved in drug
inactivation and apoptosis suppression 1.
Extrahepatic metabolism: anticancer agent inactivation
can occur in the lung, gut, kidney, urinary bladder and skin 1.
Excretion of anticancer agent occurs through two main routes:
biliary and renal excretion 1.
Biliary or bile duct excretion: Overexpression of ABC
increase the biliary excretion of anticancer agent 1.
Renal excretion: an increase in the glomerular
filtration rate (GFR) reduces the availability of anticancer drug 1.
Administration of a single chemotherapeutic agent is not
effective. Since, high concentration of the agent is needed, plus it causes
more toxicity, increase the likelihood of resistance and attack only single
population of tumor (a tumor consists of a heterogeneous population) 1.
However, using a combination of chemotherapeutic agents is effective. Since, it
decreases the required concentration for each agent, decreases the side
effects, decreases the likelihood of resistance and attack several population
of the tumor 1.
Microscopic (local) resistance tumor related factors
Ineffective chemotherapy can occur at the tumor site 1.
This happens by several mechanisms. Some of them are:
Also called acquired resistance, extrinsic resistance, active
resistance, or biochemical resistance 1. Evolutionary resistance could occur
either through manipulating drug resident time inside the cell and/or modifying
its site of action 1.
1. Alteration of drug residency in cancer cells
Proteins are the main reason for altering drug residency in
cancer cell, including:
· P-gp: Some anticancer agent is inactivated
through CYP3A4 due to its expression by P-gp 1. Expression of P-gp fluctuates
with increased expression level in untreated cancer into higher level upon
relapse after chemotherapy and undetectable or decreased level in the
expression in drug sensitive tumors 1.
MRPs (Multidrug resistance-associated protein): MRPs are very much alike to P-gp
being (1) able to decrease drug concentration inside the cell and (2)
MXR (Mitoxantrone resistance protein): is one member of the ABC-superfamily
that is involved in exchanging biological molecules across cell membranes 1.
If cancer cells don’t have P-gp and MRP to elicit chemotherapy resistance,
expression of MXR can be a substitute strategy 1.
2. Alteration of drug target
Another mechanism of resistance may emerge when the drug
arrives at its site of action. 1. This type of mechanism of resistance can be
made clear by these examples:
DNA topoisomerase II mutations result in resistance to
drugs that act on this enzyme such as doxorubicin and etoposide 8.
Dihydrofolate reductase amplification result in
resistance to drugs that act on this enzyme such as methotrexate 9.
Cancer cells have different microenvironment than normal
cells. For example, the pH is less than seven extracellularly and more than seven
intracellularly 1. Due to the different microenvironment that cancer cells
posses, they have the capacity to decrease immunity, stop normal cell growth and
prevent drugs entry to cancer cells. 1. There are three important components
of cancer cell microenvironment that grant drug restriction 1:
Anticancer agent undergoes “ion
trapping mechanism”, where weakly basic anticancer agents partitioning to
cancer cells are decreased due to its ionization at the interstitial fluid and
their incorporation into the lysosomes after they cross the plasma membrane 1.
And, where weakly acidic anticancer agents partitioning to cancer cells are
increased and rendered after they cross the plasma membrane, slightly prevented
from reaching the target site 1.
Hypoxia causes chemotherapy resistance by eliminating the presence of
free radicals, which is important to initiate apoptosis of cancer cells 1.
Hyperglycemia may have an impact on
the effectiveness of chemotherapy 5.
Mesoscopic (physical, mechanical) or (regional) resistance
tumor—host interacting factors
Blood vessel morphology and blood viscosity at tumor site
affect chemotherapy efficacy 1. Increase vascular resistance and blood
viscosity results in a decrease of the amount of anticancer agent reaching
their target site and vice versa 1.