IP International Journal of Comprehensive and Advanced Pharmacology 2023;8(1):27–31
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IP International Journal of Comprehensive and Advanced
Pharmacology
Journal homepage: https://www.ijcap.in/
Review Article
A comprehensive review on preliminary screening models for the evaluation of
anti-cancer agents
Bhargav K Kamani
1
, Keval Y. Raval
1,
*
1
Dept. of Pharmacology, School of Pharamcy, RK University, Tramba, Gujarat, India
ARTICLE INFO
Article history:
Received 23-10-2022
Accepted 25-12-2022
Available online 27-03-2023
Keywords:
Cancer
Invivo
invitro
Anticancer drug
Screening methods
ABSTRACT
Cancer refers to a category of illnesses characterised by uncontrolled growth of new cells. The screening
of an anticancer drug is a time-consuming procedure that requires several in-vitro, in-vivo, and clinical
investigations. Toxic dosages of screening pharmaceutical drugs in-vivo at varying concentrations need
to be envisioned in order to prevent chemical poisoning in animals throughout an experiment. Cancer
management has been the subject of several in-vitro and in-vivo investigations. To determine the test
compound’s anti-cancer efficacy, this research compiled a review of in vivo and in vitro assays. Here,
the study emphasizes on the numerous preclinical approaches and processes used in anticancer research.
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1. Introduction
In the past two decades, biological factors have taken
the role of empiric chemical factors in the discovery and
development of novel anti-cancer drugs. These factors are
mostly based on compounds that operate on molecular
targets. This is the outcome of increased biological
understanding of the molecular pathways that have been
discovered to be dysregulated and/or over-activated in
various tumors, which has resulted in the identification
of molecular targets such as growth factor receptor and
intracellular signaling molecules against which drugs have
been developed.
1
This increased biological knowledge has
been associated with development of high-throughput
genomics and compound screening that allow development
of drug which interact with above mentioned targets.
2
Identification of new anti-cancer agents is mainly based on
in-vitro methods, the in vivo models are absolutely required
to assess the pharmacological activity of a potential new
drug in animal models.
3
* Corresponding author.
E-mail address: keval.raval@rku.ac.in (K. Y. Raval).
The development of a new anti-cancer agent involves
several steps including in-vitro assays, both cells based and
molecular target-driven, for the identification of an active
compound and in-vivo studies to evaluate the potential
anticancer activity; pharmacological studies to evaluate
drug absorption, distribution, metabolism, and elimination;
and, toxicological studies.
4
We understand that the conceptual distinction between
traditional cytotoxic agents and targeted drugs is frequently
incorrect and deceptive, given that the majority of cytotoxic
agents do indeed have well-defined targets, such as DNA
or tubulin, and that the majority of new agents are instead
directed at non-cancer-specific targets, such as enzymes or
factors expressed in both normal and cancer cells. Figure
1 elucidates the preclinical developmental steps for the
screening of anti-cancer agents.
Here we presented the theoretical information on the
preclinical experimental models that are available in this
work to assess either drugs with non-cancer-specific targets
or those that have been utilized to establish such targets.
There are number of models are available to evaluate the
same and described below.
https://doi.org/10.18231/j.ijcaap.2023.004
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