Role of chromosomal cohesion and separation in aneuploidy and tumorigenesis

Cell division is a crucial process, and one of its essential steps involves copying the genetic material, which is organized into structures called chromosomes. Before a cell can divide into two, it needs to ensure that each newly copied chromosome is paired tightly with its identical twin. This pairing is maintained by a protein complex known as cohesin, which is conserved in various organisms, from single-celled ones to humans. Cohesin essentially encircles the DNA, creating a ring-like structure to handcuff, to keep the newly synthesized sister chromosomes together in pairs. Therefore, chromosomal cohesion and separation are fundamental processes governing the attachment and segregation of sister chromatids during cell division. Metaphase-to-anaphase transition requires dissolution of cohesins by the enzyme Separase. The tight regulation of these processes is vital for safeguarding genomic stability. Dysregulation in chromosomal cohesion and separation resulting in aneuploidy, a condition characterized by an abnormal chromosome count in a cell, is strongly associated with cancer. Aneuploidy is a recurring hallmark in many cancer types, and abnormalities in chromosomal cohesion and separation have been identified as significant contributors to various cancers, such as acute myeloid leukemia, myelodysplastic syndrome, colorectal, bladder, and other solid cancers. Mutations within the cohesin complex have been associated with these cancers, as they interfere with chromosomal segregation, genome organization, and gene expression, promoting aneuploidy and contributing to the initiation of malignancy. In summary, chromosomal cohesion and separation processes play a pivotal role in preserving genomic stability, and aberrations in these mechanisms can lead to aneuploidy and cancer. Gaining a deeper understanding of the molecular intricacies of chromosomal cohesion and separation offers promising prospects for the development of innovative therapeutic approaches in the battle against cancer.


Introduction
Cells serve as the fundamental units of our bodies, and they divide through complex processes like mitosis and meiosis.These processes involve a series of intricate steps that culminate in the replication and separation of the cell's genetic material with very high fidelity, ultimately yielding two genetically identical daughter cells [1].
A critical aspect of mitosis is the faithful replication of the cell's DNA during the S phase.Following this, sister chromatids, which are pairs of replicated chromosomes, are held together by a remarkable group of proteins known as the cohesin complex [2].This complex acts as a molecular glue, maintaining the cohesion of sister chromatids until the metaphase of cell division [3][4][5].During the transition from metaphase to anaphase, the replicated chromosomes are meticulously separated after the removal of the cohesin complex [6,7].This process ensures the precise distribution of genetic material into each daughter cell [8].Any malfunction in this process can result in chromosomal anomalies leading to abnormal chromosome content, known as aneuploidy, and more likely to result in cell death.However, the cells that overcome the aneuploidy stress can result in uncontrolled cell growth, a defining characteristic of human tumors [9][10][11][12].Understanding the mechanisms that govern chromosomal cohesion and separation is therefore vital for comprehending how cells preserve genomic fidelity.

Discovery of cohesin
Historically, it was thought that DNA catenation, a process where sister chromatids are intertwined at specific sites during DNA replication, held them together, much like twisted threads, and this connection needed to be unraveled at anaphase by enzymes known as type II topoisomerases [13].In 1987, a seminal study from the Hartwell laboratory [14] provided the first evidence against the catenation model, prompting the search for factors responsible for holding sister chromatids together.However, a pivotal discovery emerged in 1997 when two independent groups of researchers made a significant discovery using genetic studies in yeast S. cerevisiae [15,16].Their discovery revealed that a group of proteins known as Structural Maintenance of Chromosomes (SMC), many of which were initially identified for their roles in DNA repair, played a primary role in keeping sister chromatids together [2][3][4].The complex formed by these proteins is now known as "cohesion".When yeast cells had mutations in the genes that encode these proteins, the sister chromatids separated too soon.This discovery was a significant leap in our understanding of how mitosis, the cell division process, works.

Composition of cohesin complex and its function
In mitotic cells, cohesin is composed of a tripartite ring containing Smc1a, Smc3, Rad21, and a peripheral subunit Scc3 in yeast that, in vertebrates, exists as two closely related isoforms: the abundant STAG2 (SA2) and the less abundant STAG1 (SA1) [2].SMC1a and SMC3 are ABC-like ATPases [17].The N-and C-terminus of SMC molecules fold back on themselves forming antiparallel intramolecular coiled coils.SMC1a and SMC3 form a heterodimer via the hinge domain [18][19][20].The C-and N-termini of RAD21 bind proximal to the head domains of SMC1a and SMC3 heterodimer, respectively, to form a triangular ring, and SCC3 (SA1/2) binds to RAD21 and SMC3 subunits to reinforce the ring [21][22][23], playing a critical role in facilitating cohesin's association with DNA [24][25][26].Moreover, these STAG subunits within the cohesin complex possess the capacity to engage with RNA within the cellular nucleus [26].
Cohesin is also located in centrosomes and plays a crucial role in centriole tethering.Similar to its proteolytic cleavage of RAD21 during the separation of sister chromatids in the metaphase-to-anaphase transition, Separase activity is also essential for the disengagement of centrioles [8].Although the exact timing and the regulatory network governing centriole disengagement remain to be fully defined, the consensus is that centriole disengagement occurs during the late mitosis/early G1 phase [51][52][53][54].This process takes place after the separation of sister chromatids, providing an additional mitotic mechanism that could impact faithful chromosome segregation.Apart from its canonical function of sister-chromatid cohesion and separation, cohesin also play roles in transcriptional regulation, DNA double-strand break repair, chromosome architecture and rearrangement, and DNA replication [23,55,56].
To activate transcription properly, cohesin loops chromatin, bringing distant regions together.Chromosomes contain conserved regulatory elements (CREs) with enhancers boosting transcription and insulators blocking it.Cohesins physically connect distant CREs with gene promoters in a cell-type specific manner.Depending upon cohesin's binding to activators or insulators, it influences transcriptional outcomes either positively or negatively.Changes in cohesin levels could impact its binding to CREs and chromatin structure, altering their interaction with promoters and, consequently, gene activity.Even a slight decrease in chromatin-bound cohesin can lead to changes in the expression of many genes.However, our understanding of how cohesin is recruited and removed from transcription sites to regulate transcription is limited.

Models of sister chromatid cohesion
Sister chromatid cohesion around the two sister chromatids is currently explained by two major models [2,[57][58][59][60].The first model, known as the "one-ring embrace", proposes that a single cohesin ring captures and holds together two sister chromatids throughout the cell cycle [2,61].Using minichromosome as a tool, Nasmyth and colleagues showed that the way cohesin and DNA connect is like a twisty knot.They did this by separating the connection between cohesin and DNA, either by cutting cohesin or cutting the DNA rings [62].Their results supported the concept that the three parts of the Smc1-Smc3-Scc3 connection resemble more of an embrace, achieved using proteins and a cross-linker to seal them together [63].However, later research findings challenge this idea.The alternative model, referred to as the "dimeric handcuffmodel," suggests a more complex scenario [24, 32, 57-59, 64, 65].According to this model, multiple cohesin molecules cooperate to generate cohesion.These cohesin molecules form two separate rings, each consisting of RAD21, SMC1a, and SMC3 protein subunits.The key concept here is the formation of a handcuff-like structure, where two RAD21 molecules within these rings align in an anti-parallel orientation.The orientation is enforced by proteins STAG1 or STAG2.Mutations in the STAGbinding motif in STAG proteins reduced RAD21-RAD21 interaction [66].When STAG1/STAG2 is inhibited, the rings disassemble, resulting in the loss of cohesion.Later findings using budding yeast as a model supported that Scc3 or Pds5 may serve as factors that structurally stabilize two cohesin rings, forming a handcuff conformation [67,68].Notably, the removal of Pds5 in cells did not result in alterations in cohesin levels on chromatin, even though changes in sister chromatid cohesion were observed.Recent studies have also provided compelling evidence for the presence of cohesin dimers in cells [24,65].Cohesin dimers, which involve two cohesin molecules working together, appear to play a crucial role in the organization of chromosomes.Despite these significant findings, our understanding of cohesin dimers and their precise role in chromosomal organization is still evolving.More in-depth research is necessary to uncover the intricacies of cohesin dimerization and its impact on chromosome dynamics during cell division.Future investigations, such as reconstructing the human cohesin complex binding to chromatin in vitro and conducting structural and microscopy studies, as well as high-throughput chromosome conformation capture (Hi-C) experiments, are expected to provide additional insights into cohesin's detailed role in regulating high-order chromatin structures and may reveal the true nature of cohesin rings in the context of cell division.

Cohesin and accurate chromosome segregation
Accurate chromosome segregation during anaphase is a fundamental process that relies on the tight regulation of cohesin [69][70][71].Cohesin maintains the connection from the moment sister chromatids are synthesized during the S phase until their separation in anaphase.During mitosis, the assembly of the spindle apparatus becomes an important event, as it engages the kinetochores of all chromosomes.Notably, the proper attachment of kinetochores to spindle microtubules, referred to as amphitelic (bi-orientation) attachment, is a key determinant in enabling the eventual separation of sister chromatids [72][73][74].This separation is executed by the enzymatic cleavage of specific cohesin subunits, namely RAD21, catalyzed by the enzyme Separase.After cohesin cleavage, sister chromatids are released and move toward opposite poles due to the action of the spindle apparatus [6][7][8] (Fig. 1).

Role of separase
It is important to recognize that the removal of cohesin, and consequently the separation of sister chromatids, is an irreversible step.Therefore, the removal of cohesin needs to be synchronized for the proper segregation of the chromatids to opposite spindle poles [8,75].Premature separation of sister chromatids can lead to aneuploidy, a condition characterized by an abnormal number of chromosomes, and potentially contribute to tumorigenesis [8,10,76,77].

The consequences of cohesin dysregulation and Separase overexpression
Despite many control mechanisms, overexpression of Separase, a feature of many human tumors including breast, prostate, bone, brain, and blood cancers [33,[83][84][85][86][87][88][89], has been reported to cause chromosomal missegregation and aneuploidy [8,33,84,90].ESPL1 is an oncogene, the transcription of which can be activated by the steroid hormones estrogen and progesterone [91], and that overexpression of Separase induces chromosomal missegregation in tissue culture, mammary transplants, and transgenic animals through premature separation of chromatids, resulting in aneuploidy and mammary tumorigenesis [33,84].The significance and relevance of these studies in mice are underscored by the finding that Separase is overexpressed in numerous human tumors.Further, overexpression of Separase strongly correlates with a high incidence of relapse and metastasis and a lower 5-year overall survival rate [8,83,85,90].Meta-analysis indicates a strong positive correlation between Separase mRNA expression and tumor grade, and a strong negative correlation with disease-free and overall survival [8,83,85,[87][88][89][92][93][94].Despite its overexpression in numerous human tumors, the role of Separase as an oncogene and its relevance as an oncotarget have been grossly understudied [8].Specifically, how Separase overexpression-driven aneuploidy overcomes the threshold of tumor-resisting forces within the cell and results in the initiation of tumor formation and how other cooperating lesions further this process need to be investigated.

Cohesin mutations and aneuploidy
Mutations in cohesin have been a subject of intense research, and their relationship with aneuploidy has generated significant interest [77], [95].Somatic mutations in genes associated with the cohesin complex and its regulators are prevalent in various cancer types, such as glioblastoma, Ewing's sarcoma, bladder cancer, and myeloid neoplasms [96][97][98][99][100][101][102][103][104][105][106][107][108][109][110][111][112].These mutations, which can range from 4 to 36% in different cancers, tend to involve genes encoding core cohesin subunits [71,[113][114][115].Interestingly, these mutations typically occur in a mutually exclusive manner, without specific hotspots identified.Among the cohesin subunits, STAG2 stands out as the most frequently mutated subunit and is implicated in four or more cancer types [111,116].Moreover, certain cases of myeloid neoplasms and Ewing sarcoma have revealed instances of reduced cohesin gene expression, even in the absence of mutations [105,110].In a parallel line of genetic alterations, mutations affecting the binding sites of cohesin and CTCF, a cohesinassociated protein, have been observed in multiple cancer types [117].It is important to note that cohesin mutations alone are insufficient to drive malignancy.Rather, they must coincide with other genetic mutations and collaborate with abnormal signaling events to contribute to cancer progression [105,106,108,112].A recent study in budding yeast found that under normal conditions, cohesin's role in maintaining cohesion between sister chromatids serves to suppress aneuploidy and prevent whole chromosome loss of heterozygosity.However, when sister chromatid cohesion becomes compromised, it can result in significant genetic consequences including whole chromosome loss of heterozygosity [118].This underscores the cooperative and context-dependent nature of cohesin mutations in the development of cancer.
Several studies have explored the impact of cohesin mutations on aneuploidy, and while a clear connection exists in some cases, the relationship is more complex in others [77].Cohesin deficiency in cell models can lead to chromosome and cell cycle irregularities.While cohesin mutations were initially expected to be linked with aneuploidy in cancers, the connection is not straightforward.Some studies found an association between cohesin mutations and chromosome copynumber variations, while others did not observe increased aneuploidy in cohesin mutant cancers, such as bladder cancer, Ewing sarcoma, or myeloid neoplasms.Interestingly, specific types of STAG2 mutations adversely affected chromatid cohesion and chromosome segregation, but this did not consistently result in a substantial increase in chromosome number [119].Reduced cohesin expression was also linked to chromosome instability in some cases, characterized by increased micronuclear formation and nuclear size [120].In summary, cohesin mutations can lead to chromosome instability in certain cases, but this does not necessarily result in aneuploidy.Therefore, the link between cohesin mutations and aneuploidy is still debated.
Several studies suggest that the primary mechanism by which cohesin mutations contribute to cancer is through disrupting genome organization and transcription impacting proto-oncogenes or tumor suppressor genes [115,[121][122][123][124][125][126][127][128][129][130][131].Dysfunctional cohesin affects its dynamic binding to chromatin and impairs the recruitment of RNA polymerase II, leading to transcriptional dysregulation.Cancer-associated mutations in cohesin genes can lead to aberrant DNA looping, dysregulation of crucial lineagespecific transcription factors, and misexpression of genes responsible for cellular identity and homeostasis [122,125,126,[131][132][133][134][135][136].Cohesin insufficiency can enhance self-renewal while impairing differentiation, leading to abnormal cellular plasticity, which is central to malignant transformation.This effect has been observed in hematopoietic stem cells, where cohesin insufficiency results in misexpression of critical genes involved in hematopoiesis [122,125,126,[131][132][133][134].In mouse embryonic stem cells, cohesin depletion reduces enhancer-promoter interactions at pluripotency genes, causing a loss of the pluripotent state [137,138].Loss-of-function mutations in STAG2, found in Ewing's sarcoma, alter dynamic loop extrusion, decrease cis-promoter-enhancer interactions, and lead to significant changes in the transcriptome [139].Replication stress, involving challenges to DNA replication fork progression, can be influenced by cohesin, which accumulates at stalled forks and facilitates template switching to repair DNA lesions [140].Cohesin depletion increases Pol II pausing at cohesinbinding genes, highlighting its role in resolving replication stress [141].STAG1 is also implicated in interactions with the Super Elongation Complex, a process linked to leukemia and multiple myeloma pathogenesis [142].Overall, cohesin defects play a significant role in cancer development, involving a complex interplay of aneuploidy, altered gene expression, and participation in DNA replication and repair processes.However, distinguishing between aneuploidy and transcriptional changes resulting from cohesin mutations is experimentally challenging, suggesting that both processes likely occur concurrently.
In summary, the connection between cohesin mutations and aneuploidy is complex and context-dependent.While some cancers show a clear link between cohesin mutations and aneuploidy, others do not, emphasizing the multifaceted role of cohesin mutations in cancer development.Understanding the specifics of these relationships is crucial for developing targeted therapies and treatments for various cancer types.

Aneuploidy and its link to cancer: an overview
Aneuploidy is a hallmark of human cancers [12,143,144].It refers to an imbalanced karyotype marked by an abnormal number of chromosomes in cells.The frequency of aneuploidy varies among different cancer types, ranging from approximately 25% in thyroid carcinomas to nearly 100% in glioblastomas [145].About 97% of breast cancers show one or more aneuploidies, where around 60% of breast cancer tumors contain an extra copy of chromosome arm 1q11, which is a more prevalent alteration compared to mutations in genes like PIK3CA (found in 39% of breast tumors) that encodes Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Alpha, or TP53 (in 34%) [145] which encodes p53 protein, a tumor suppressor.Aneuploidy's exact causes remain unclear, but it can indirectly lead to changes in gene expression from trisomic and monosomic chromosomes.In contrast, healthy, non-cancerous cells in the human body are typically very strict about maintaining the right number and structure of chromosomes during cell division.This key difference between cancer cells and normal cells has given rise to the hypothesis that cancer cells have somehow developed the ability to overcome inherent barriers to changes in chromosomes that normal cells cannot tolerate.This means that they have acquired unique strategies to deal with these genetic alterations.However, what this strategy is currently remain undefined.

Aneuploidy's dual role: neither universal oncogenic nor tumor suppressor
Aneuploidy frequently develops early in tumorigenesis [146-151] with some chromosomal alterations occurring later in tumor development, potentially after cells have acquired mutations allowing them to tolerate aneuploidy's effects [152].On the other hand, considering that in most cases, aneuploidy can be detrimental to cell fitness, it is possible that aneuploidy serves as an early evolutionary response to counteract uncontrolled cell division triggered by factors, such as oncogenic mutations, epigenetic changes, or environmental stress.The fact that many aneuploidies are capable of functioning as tumor suppressors [12] supports this alternate hypothesis.However, as cells face repeated oncogenic challenges, they may adapt to tolerate aneuploidy through genetic or epigenetic alterations that support uncontrolled growth.Evidence for this concept comes from observations that aneuploid cells can acquire mutations enhancing their proliferative capacity, such as in the ubiquitin-proteasome pathway of budding yeast [153].In mammalian cells, the loss of the tumor suppressor p53 has been shown to facilitate the growth of aneuploid cells [12,154,155].In a model of hormone-induced spontaneous tumorigenesis in p53-null mammary glands, our research has revealed that the rate of chromosome missegregation can be significantly influenced by changes in the levels of two crucial proteins: Separase and MAD2, which play essential roles in maintaining proper chromosomal segregation and the spindle checkpoint during mitosis [91].As tumor progresses, cells counter-evolve and further adapt to tolerate aneuploidy through significant chromosomal and genomic alterations, enabling them to meet the demands of uncontrolled tumor growth.
The precise mechanisms governing aneuploidy tolerance and the shift from aneuploidy's anti-tumorigenic traits to cancer-promoting features remain elusive.The ways in which cancer cells maintain vigorous growth despite highly aneuploid karyotypes are still actively under investigation and lack a comprehensive understanding.In some rare instances, aneuploid karyotypes may exhibit properties that benefit cancer development, such as immune evasion, drug resistance, and the overexpression of oncogenes.These advantageous aneuploidies can gradually become more prevalent within the tumor as they are selectively favored over time [12].

Chromosomal instability and aneuploidy
Chromosomal instability (CIN) and aneuploidy are intricately connected in cancer [156,157].While one can be considered the cause, the other is the resulting effect.Aneuploidy characterizes an unbalanced chromosomal arrangement, whereas CIN is a state in which cells frequently missegregate whole chromosomes, thus playing a role in the development of aneuploidy [156,158].While CIN can give rise to aneuploidy, aneuploidy can lead to CIN.Similarly, like that of aneuploidy, CIN can also exert both tumor-promoting and tumor-suppressive effects [12].The mechanisms of chromosomal instability have been extensively covered in several excellent reviews [159][160][161][162], but the outcome is consistently the missegregation of chromosomes.Missegregated chromosomes do not always result in aneuploidy but can trigger various other effects.
These include DNA damage, activation of the cytosolic DNA-sensing pathway involving cyclic GMP-AMP synthase (cGAS) and stimulator of interferon genes (STING), and chromothripsis, a phenomenon where one or more chromosomes shatter and are incorrectly reassembled [163][164][165][166][167]. Hence, these CIN can impact tumorigenesis through mechanisms that are independent of aneuploidy.

Consequences of aneuploidy
Aneuploidy, through the gain or loss of whole chromosomes, creates imbalances in the proteome [162,168], particularly in proteins crucial for DNA metabolism and cell cycle regulation, elevating the risk of DNA mutations [169][170][171].Single-chromosomal aneuploidy in budding yeast producing a modest, but significant, elevation in the rates of point mutations and mitotic recombination supports this notion [172].Aneuploidy-driven genome instability could arise from chromosome missegregation errors in mammalian cells, which leads to double-strand breaks as a result of lagging anaphase chromosomes trapped in the cleavage furrow during cytokinesis [10,173].In addition to the damage caused directly by the mitotic machinery, lagging chromosomes, including those that are not missegregated, often form micronuclei, which also accumulate high levels of DNA damage resulting in chromosome fragmentations or shattering leading to chromothripsis [10,[174][175][176][177][178].While epigenetic dysregulation is recognized as a factor in cancer [179,180], its connection to aneuploidy remains a lessexplored area.
Aneuploidy can influence the behavior of oncogenes and tumor suppressors without triggering an immune response.Additionally, aneuploidy can change the expression of antigens and cell surface markers, creating a diverse range that helps certain cells evade immune detection.As indicated earlier, a related feature, chromosomal instability, can activate pathways like cGAS-STING, leading to a phenomenon called the senescence-associated secretory phenotype (SASP) [181].While SASP can aid the immune system, particularly natural killer cells, in recognizing and eliminating aneuploid cells, it can also contribute to tumorpromoting behaviors such as mesenchymal transitions, chronic inflammation, and the release of factors that support tumor growth [12].This intricate relationship between aneuploidy, the immune system, and tumorigenesis is currently a subject of active investigation.
Aneuploidy can arise from various cellular defects, including issues with the spindle apparatus, centrosome and centriole abnormalities, checkpoint maintenance, and altered telomere and centromere stability [10].These defects can occur spontaneously or be induced by mutations in relevant genes, potentially causing aneuploidy.Recent studies demonstrate that aneuploidy alone can trigger mutations that drive cancer initiation and progression [156,182,183].However, the full spectrum of mutations and epigenetic changes associated with aneuploidy in the context of tumor development remains a subject of ongoing investigation.

Aneuploidy and cancer therapy: a promising avenue
Surprisingly, despite being a consistent feature of human tumors, aneuploidy status has not been harnessed for cancer therapy.Aneuploidy, a common feature in various cancers but rare in normal tissues, presents a promising target for cancer treatment.This distinction between cancerous and healthy tissues holds the potential for a captivating avenue in cancer therapy, where aneuploid cancer cells could be selectively targeted while sparing normal, diploid cells, thus reducing side effects.This innovative approach holds promise for a wide spectrum of cancer types [184].
One avenue of exploration is to exploit the inherent vulnerability of untransformed aneuploid cells to certain metabolic stressors.Studies have shown that aneuploid cells are more sensitive to the activation of the AMP-activated protein kinase (AMPK) and peroxisome proliferatoractivated receptor-γ co-activator 1α (PGC1α) pathway [185,186].This pathway plays a central role in regulating energy metabolism and mitochondrial biogenesis.Aneuploid cells are already under considerable energy stress, and further disruption of these metabolic pathways may push them over the edge, causing toxic levels of metabolic dysregulation.Additionally, aneuploid cells have higher levels of ceramide, a type of lipid molecule, and further elevating ceramide levels is significantly more toxic to aneuploid cells compared to diploid cells [187].
Another approach to targeting aneuploid cancer cells is to exacerbate their chromosomal mis-segregation [188].Since aneuploidy and chromosomal instability (CIN) are closely intertwined, increasing the rate of chromosome missegregation beyond tolerable levels may specifically compromise the viability of aneuploid cells.Many aneuploid cancer cells exhibit altered microtubule dynamics and increased stability of microtubule-kinetochore connections.These spindle disruptions can result in improper kinetochore attachments, hinder error correction mechanisms, and lead to high levels of chromosome missegregation.Inhibiting the spindle-assembly checkpoint has been shown to selectively kill aneuploid cancer cells by further enhancing their level of CIN [189][190][191][192].
Furthermore, recent research suggests that aneuploid cancer cells may be sensitive to spindle disruption by inhibiting a mitotic kinesin, even without a complete loss of the spindle-assembly checkpoint [192].Specifically, the mitotic kinesin KIF18A, which is generally dispensable for most mammalian cell proliferation, appears to be more toxic to aneuploid cells compared to diploid cells [193,194].Knockdown of KIF18A in cells with highly aneuploid karyotypes leads to alterations in spindle geometry and microtubule dynamics, resulting in mitotic errors, micronucleus formation, and a reduction in cellular viability.
These findings suggest that KIF18A inhibition could hold promise as a target for future drug development aimed at establishing anti-aneuploidy therapeutic strategies for cancer treatment [195].Overall, these approaches offer exciting possibilities for selectively targeting aneuploid cancer cells, providing new avenues for developing effective and targeted cancer therapies.

Separase: an innovative target to tackle aneuploidy
During cell division, Separase's enzymatic activity is brief and requires minimal active enzyme levels to cleave cohesin molecules [50,196].Therefore, unlike other mitotic targets, pharmacologic inhibition of Separase by small molecule drugs presents an effective strategy to be a more effective mitotic target in inhibiting the proliferation of cancer cells addicted to Separase overexpression without affecting the normal cell division [8].
Knockdown of Separase inhibits the growth of breast cancer cells while sparing normal mammary epithelial cells.Small molecule inhibitors of Separase, known as Sepins, have been identified and shown to be effective in selectively targeting Separase-overexpressing cancer cells in culture and in xenograft studies [200].Therefore, Separase represents an ideal therapeutic target to eliminate Separase-overexpressed aneuploid tumors including various breast tumor subtypes, and Sepins offer a promising avenue for breast and other cancer therapeutics.

Conclusion and future prospective
To conclude, the intricate processes of chromosomal cohesion and separation play pivotal roles in governing genomic integrity and fidelity, making them key players in the complex landscape of cancer biology.Any malfunction in this process can result in chromosomal anomalies, leading to abnormal chromosome content, a condition known as aneuploidy.Aneuploidy is a defining characteristic of human tumors and contributes significantly to the initiation and progression of cancer.Overexpression of Separase has been linked to chromosomal missegregation, aneuploidy, and tumorigenesis.Thus, the level of Separase activity is a crucial determinant of genomic stability.Notably, Separase has emerged as an innovative therapeutic target to tackle aneuploidy in cancer.Small molecule inhibitors of Separase, known as Sepins, show promise in selectively targeting Separase-overexpressing cancer cells while sparing normal cells.This targeted approach offers a novel avenue for cancer therapy, potentially reducing side effects and improving the prognosis for various cancer types, particularly those with high Separase expression.
The intricate relationship between aneuploidy, chromosomal instability, and cancer also remains a topic of ongoing investigation, offering a fertile ground for future research.As we uncover more details about the mechanisms and consequences of aneuploidy in cancer, we move closer to the development of innovative and targeted therapies that could improve the prognosis for a wide range of cancer types.
In summary, the roles of chromosomal cohesion and separation in the context of aneuploidy and cancer are tightly intertwined.The precise regulation of these processes is essential to maintain genomic stability, and their dysregulation can lead to aneuploidy, a hallmark of cancer.By targeting key players like Separase, we may pave the way for innovative and effective cancer therapies that specifically address the unique vulnerabilities of aneuploid cancer cells, offering hope for improved cancer treatment outcomes.