Breast cancer has been identified as one of the main cancer-related deaths among women during
some last decades. Recent advances in the introduction of novel potent anti-cancer therapeutics in association
with early detection methods led to a decrease in the mortality rate of breast cancer. However, the scenario of
breast cancer is yet going on and further improvements in the current anti-cancer therapeutic approaches are
needed. Several factors are present in the tumor microenvironment which help to cancer progression and suppression
of anti-tumor responses. Targeting these cancer-promoting factors in the tumor microenvironment has
been suggested as a potent immunotherapeutic approach for cancer therapy. Among the various tumorsupporting
factors, Cyclin-Dependent Kinases (CDKs) are proposed as a novel promising target for cancer therapy.
These factors in association with cyclins play a key role in cell cycle progression. Dysregulation of CDKs
which leads to increased cell proliferation has been identified in various cancers, such as breast cancer. Accordingly,
the development and use of CDK-inhibitors have been associated with encouraging results in the treatment
of breast cancer. However, it is unknown that the inhibition of which CDK is the most effective strategy
for breast cancer therapy. Since the selective blockage of CDK1 alone or in combination with other therapeutics
has been associated with potent anti-cancer outcomes, it is suggested that CDK1 may be considered as the best
CDK target for breast cancer therapy. In this review, we will discuss the role of CDK1 in breast cancer progression
and treatment.
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