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Most of the human malignant neoplastic diseases begin at the degree of familial mechanisms where normal cell rhythm is disrupted or unnatural reproductions of familial stuff spell unbridled. Either the increased degree of cellular proliferation or decreased degree of apoptotic tract will disrupt the homeostasis of cells and breed the niche for possible tumorigenesis. Attributed as a defender of the genome, p53 protein is good recognized in stamp downing tumor development as in cell rhythm control, apoptotic tract, and DNA fix mechanism. Functioning as a tumor suppresser protein, the degree of p53 is tightly controlled by MDM2 protein. The p53 dependent mechanism of MDM2 protein regulates p53-mediated transcriptional activity in two ways, foremost MDM2 protein binds to p53 transcriptional activation sphere ( TAD ) doing it transcriptionally inactive and secondly debasement of p53 in the cytol by moving as an E3 ubiquitin ligase. MDM2 cistron look is in bend controlled by active p53 protein through a p53 antiphonal booster ( P2 ) located in first noncoding DNA of this cistron. Therefore, MDM2-p53 autoregulatory cringle forms a finely balanced regulative web and if it is disrupted, the balances of the proteins are out and the cells become more susceptible to malignant neoplastic disease. Following exposure of extracellular and intracellular stimulations that causes DNA harm such as ionising radiation, DNA harm, hypoxia, infective viruses, p53 protein is stabilized in the karyon and its association with MDM2 is disrupted by either post-translational alterations of proteins or intervention of MDM2 map by p19ARF. In this manner, elevated degree of p53 proteins activate the cistrons possessing p53 antiphonal elements and carried out its map.

MDM2 has non merely p53 dependent maps but it besides has some p53 independent maps which are besides critical for carcinogenesis. MDM2 protein can straight adhere with pRb protein and E2F1 ( E2F transcriptional factor 1 ) advancing G1 to S stage patterned advance of the cells through disrupting pRb every bit good as exciting E2F1 maps. In response to DNA harm, p21 protein which is a cyclin dependent kinase inhibitor is up-regulated ensuing in G1 stage cell rhythm apprehension. MDM2 can besides move as a negative regulator for p21 protein by advancing its proteasomal debasement in the nucleus via p53 independent tract. Furthermore, MDM2 protein is an indispensable property for ubiquitylation and debasement of certain steroid endocrine receptors known as glucocorticoid receptor, androgen receptoron the other manus it can heighten the estrogen dependent written text through estrogen receptor I± ( ERI± ) .

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MDMX/MDM4, a structurally similar protein with MDM2 particularly in the N-terminal p53 adhering sphere and C-terminal sphere, is a well-known MDM2 household member. MDMX/MDM4 protein binds to transactivation sphere of p53 protein and interfere its map. Furthermore, MDMX/MDM4 protein can besides adhere with MDM2 protein through ring finger sphere in C terminus part and upon this hetero-oligomerization, the stableness of MDM2 is well increased. On the other manus, there is a at odds fact about MDMX that it does non hold nucleocytoplasmic shuttling map thereby impeding MDM2 mediated p53 protein debasement by making a atomic pool.

Knockout mice of MDM2 cistron are lethal in their developmental phase due to p53 dependent inordinate programmed cell death but dual smasher mice for both MDM2 and p53 survive which shows the strong grounds for MDM2 ordinance of p53 stableness in vivo. Knockout mice of MDMX/MDM4 cistron can besides lethal in embryologic phase whereas the defect is in proliferation but non apoptosis as in MDM2 cistron. Recent find of individual nucleotide polymorphism ( SNP ) at 309th place in MDM2 cistron booster sheds a new visible radiation on how SNP309 could play a function in lending to the development of malignant neoplastic diseases. The relationship between SNP309 in MDM2 cistron booster and possible tumor development will be exhaustively discussed in this reappraisal and table1, 2.

Since SNP 309 is a of course happening polymorphism, non a mutant, it can be normally found in general population. By utilizing 300 base brace from genomic DNAs isolated from 50 healthy voluntaries, SNPs have been detected in two places, at nucleotide 309th and at 344th in MDM2 booster. SNP 344 is a alteration of base from T to A and it is seldom seen among general population which is merely 8 % for heterozygous province therefore no farther surveies are done. Whereas, SNP309 polymorphism is a T to G fluctuation at the 309th base in the first noncoding DNA of the intronic booster of MDM2 cistron and it has comparatively high frequence, 40 % for heterozygous province T/G and 12 % for homozygous G/G.

The presence of SNP309 in the booster of MDM2 cistron extends the length of one of the putative DNA binding sites for the transcriptional activator viz. stimulatory protein 1 ( Sp1 ) and besides increases the adhering affinity of it. Sp1 is a co-activator of assorted endocrine receptors including ER and it contains estrogen response component ( ERE ) in its venue so it is known to be one of the participants in estrogen mediated cistron written text. Therefore, SNP309 in MDM2 cistron booster may change the effects of endocrines such as estrogen in human tumor. The degrees of MDM2 RNA and protein go higher and subsequent fading of p53 protein and malignant neoplastic disease formation can be seen ( Figure 1 and 2 ) . Overexpression of MDM2 protein leads to functional inactivation of wild-type p53 protein doing higher incidence for earlier age of oncoming, increased hazard and hapless endurance of both familial and sporadic malignant neoplastic diseases in different tissues.

The frequences of MDM2 SNP309 are varied depending on the race and ethnics. Recent surveies described that G allelomorph was assumed to be descended from the Caucasians to African Americans due to migrations of human out of Africa and alloy with Caucasians, therefore the frequence of G allelomorph seemed to be higher in Caucasians. Selective force per unit area on SNPs in p53 cistron could be possible because p53 takes portion in tumour suppression, embryologic development and even responds to rednesss, therefore infections may besides play a function in this choice.

The different frequences for other ethnics are besides discussed in many surveies and noted that the per centum of SNP309 G allelomorph was higher in Ashkenazi Jewish whereas it is lower in Caucasians. One survey stated that in Asiatic population, the frequence for G allelomorph was elevated than that of Caucasians. Since allele frequences are different among ethnics, races and population, the confounding consequence could be seen if the Numberss of patients from one cultural group are dominant over other opposite numbers in the sample being studied.

From this information, we can speculate that Ashkenazi Jewish and Asian have the highest per centum of SNP309 G allelomorph. Therefore, these two cultural groups might hold more important cancerous alterations in association with SNP309 G allelomorph than those with other population. For these grounds, it is of import to see the race and cultural group in each survey and important to compare the same race and cultural population to acquire more accurate results.

Research workers can non except the consequence of SNP309 G allele entirely on assorted types of malignant neoplastic disease by analysing the association with carcinogenesis. Associated factors, for illustration, TP53 mutant, steroid receptor position, environmental emphasis ( smoke, dietetic carcinogen, chronic viral infection ) , gender position, race & A ; ethnicity, functional polymorphisms in p53-MDM2 related cistrons and other familial sensitivities besides have to be considered. It was shown in many surveies that these associated factors play a important function in clip of tumour oncoming. “ Age-specific incidence of malignant neoplastic disease is dependent on the figure of rate-limiting mutants required for a given malignant neoplastic disease, the mutant rate per mitosis and the net proliferation rate of the accomplished cells ” . p53 cistron has an influence on all three factors and suppression of the p53 tract by SNP309 could impact all three factors and leads to acceleration of tumour formation. In this manner, SNP309 acts as a rate restricting factor in tumorigenesis. In this reappraisal, the relationship between SNP309 and different types of malignant neoplastic diseases based on their associated factors will be discussed.

An autosomal dominant malignant neoplastic disease predisposing syndrome named Li-Fraumeni syndrome ( LFS ) is normally associated with p53 germline mutant and is characterized by happening of heterogenous types of tumours at immature age. The presence of SNP309 G allelomorph in LFS patients has a distinguishable influential consequence on earlier oncoming of tumour visual aspect. In one survey, from 41 unrelated LFS households, 61 patients who have p53 germline mutant were collected to analyze the consequence of SNP309. Suprisingly, G allele bearers ( T/G or G/G ) were about 10 old ages earlier age of tumor oncoming than homozygous T allelomorph bearer ( T/T ) patients. This consequence reveals the fact that G allelomorph of SNP309 behave as a genetically modifying factor in TP53 mutant patients. There is besides another interesting point that the polymorphism identified in coding part of p53 cistron had an associated issue with SNP309. G allelomorph of SNP309 and Arg allelomorph of p53 codon72 polymorphism had a combination consequence on this tumorigenesis.

In one study, the determination showed that SNP309 G allelomorph had an earlier age of oncoming for tumor with p53 germline mutant bearers than those with T allelomorph bearers, on the other manus, in the instance of TP53 negative LFS and LFS related patients ; the difference for age of tumour oncoming was undistinguished between G allelomorph and T allele groups. Therefore, SNP309 may non move as an accelerating factor for TP53 negative LFS patients and the consequence for earlier age of oncoming for p53 mutant bearer is consistent with that of Bougerad et al. , 2005.

One study studied with 88 persons from LFS households who carry germline p53 mutant in one allelomorph and the result indicated that the earlier oncoming of tumor can be found in both homozygous ( G/G ) and heterozygous ( T/G ) SNP309 carriers.In LFS standards, multiple primary tumours can develop throughout the life clip. The most frequent tumours can be found in these patients are soft tissues sarcomas, breast malignant neoplastic disease and osteogenic sarcoma. In patients with either heterozygous or homozygous G allelomorph of SNP309, the incidence of multiple tumor appeared in a life clip was significantly more than those with T/T genotype. From these consequences, SNP309 has an impact on the two critical points of LFS, viz. the age of tumour oncoming and the manifestation of multiple tumours in life. Although SNP309 seems to play a function in age of oncoming of tumors with p53 germline mutant merely, it is besides involved in other malignant neoplastic diseases without p53 mutant. This type of malignant neoplastic disease missing p53 mutant is observed in sporadic malignant neoplastic diseases and proved in sporadic soft tissue tumor ( STS ) patients by Bond et Al.

Overall, SNP309 influences the age of tumour oncoming with p53 germline mutant bearer patients ( familial ) and it may besides hold an consequence on those without this mutant ( sporadic ) .

In chest malignant neoplastic disease, estrogens play a major function in cell growing and proliferation whereas glucocorticoids exert opposite action. Overexpression of MDM2 caused by variant SNP309 G allelomorph works together with these steroid endocrine receptors in heightening tumorigenesis. MDM2 mediates glucocorticoid receptor ( GR ) debasement through ubiquitylation. In ER positive cells, the rate of carcinogenesis is significantly high compared to those with ER negative because estrogen can heighten MDM2 written text by enrolling ER to MDM2 booster in E2 dependent mode. Furthermore, MDM2 can besides physically interact with ER and trip estrogen dependent written text. For these grounds, the patients who have both SNP309 G allelomorph and ER positive become increased hazard, earlier age of tumour oncoming and hapless forecast than others.

Recently, analysis on 658 Caucasians, Ashkenazi Jewish cultural adult females with sporadic invasive ductal chest carcinoma ( IDC ) elucidated that adult females with high ER degree who had G/G genotype were 7 old ages earlier age of oncoming than those with T/T genotype, on the contrary, adult females with low ER degree had no obvious differences between G and T allelomorph. Besides, the mean age of tumour oncoming for most of the adult females was below 51 old ages ( before climacteric ) when the degree of estrogen became the highest degree and the frequence of G allelomorph was besides higher in those premenopausal adult females than postmenopausal 1s. To corroborate this, another independent survey was done with sample size 258 Caucasic adult females, non selected for Ashkenazi Jewish ethnic and the findings were the same.

The possible nexus between chest malignant neoplastic disease with BRCA1/2 bearers and SNP309 is another interesting issue and there are a assortment of inconsistent findings on that. Yarden et Al, 2008 stated that SNP309 G allele serve as a qualifier and gas pedal of chest malignant neoplastic disease in patients with mutant BRCA1/2 cistron. On the other manus, the result another survey with British population showed that in BRCA1 bearers, there was no association with either acceleration or incidence and this polymorphism.

In add-on, SNP309 appears to impact the hazard, age of oncoming for chest malignant neoplastic disease variously in heterogenous population. Sun et Al analysed a Chinese population and observed that both hazard of tumour incidence and age of oncoming were increased in homozygous ( G/G ) genotype bearer adult females. One experiment with Chinese population showed that there was no important association between SNP309 G allelomorph and chest malignant neoplastic disease ( Ma et al. , 2006 ) . The hazard of happening chest malignant neoplastic disease in both Whites and African-Americans was non observed but the malignant neoplastic disease happening age was earlier in those patients with p53 mutant. In British dwellers, groundss for early age of oncoming of G allelomorph bearers could non detected. The hazard of malignant neoplastic disease for SNP309 was examined in Turkish abode and besides no association was found. Furthermore, one survey with German population found that non merely the hazard but besides age of oncoming for chest malignant neoplastic disease was unrelated with the polymorphism of SNP309.

To reason, G allelomorph of SNP309 in MDM2 cistron booster and steroid receptors signalling has a strong relationship in predisposing to malignant neoplastic disease. SNP309 polymorphism entirely can non hold much impact on chest malignant neoplastic disease and other extra familial discrepancies are besides indispensable to acquire the dominant result. Besides, these inconsistent findings may besides be due to different cultural groups of surveies and their different environmental backgrounds.

In CRC, SNP309 G allelomorph besides takes portion an interesting function in predisposing tumor. SNP309 with p53 wild-type ( WT ) gives rise to earlier age of tumour oncoming but non for those with p53 mutation. This was confirmed with entire 153 Italian white CRC patients, among them 77 patients were with wild-type p53 and 76 with mutant p53. In WT p53 group, patients with G/G discrepancy were about 10 old ages earlier in age of oncoming than their opposite numbers T/T genotype. In contrast, mutant p53 group did n’t demo any noteworthy difference in age of oncoming between G/G and T/T genotypes. These findings can be dependable because mutation p53 itself can take to malignant neoplastic disease and the effect of SNP309 G allelomorph is masked when it is together with p53 mutant, on the contrary, when p53 position is wild-typed, the consequence of SNP309 becomes comparatively seeable.

Most of the surveies unusually showed that some factors are concerned with SNP309 in carcinogenesis. One research evaluated that oestrogen played a portion together with SNP309 G allelomorph in tumour acceleration. In 165 Italian patients, of which 98 male and 67 female with CRC were tested. Then, it was found that the frequence of G allelomorph was enriched specifically in adult females non in work forces. The information showed that in work forces, there was no distinguishable fluctuation in age of oncoming between T and G allelomorph. But in female patients, independent of the G allelomorph position ( homozygous or heterozygous ) , age of oncoming was evidently earlier about 9 twelvemonth norm than T allelomorph and despite the position of p53 ( wild-type or unknown ) , the dominant consequence on female was consistent.

Another paper besides strongly proved that in Finnish CRC patients, adult females bearing SNP309 G allelomorph were somewhat earlier in age of tumor oncoming than those with work forces. However, one paper stated that SNP309 G allelomorph did non hold a dominant consequence on age of oncoming of CRC in both sexes. Although there are some contradictory issues upon age of oncoming among genders, the consequence of SNP309 entirely can non be excluded and estrogen may confabulate as a modifying factor of SNP309 as in chest malignant neoplastic disease.

To sum up the overall facts, SNP309 may be a qualifier for age of oncoming in CRC particularly in female gender and those with WT p53. But the correlativity between the hazard, incidence, return of CRC in patients and SNP309 G allelomorph can non be verified. For these grounds, SNP309 may move as a low penetrance susceptibleness tumor marker in CRC.

Unlike other tumors, it is critical to take into history the histology of tissue beginning in lung malignant neoplastic disease. Depending on the histology, the response and result of tumor can be different so tissue specific nature of SNP309 polymorphism plays a critical function. The correlativity between SNP309 and lung malignant neoplastic disease based on different races, smoking position, gender, age of patient and histology types were extensively studied.

In one survey, 1,106 Chinese patients were divided into three groups harmonizing to the histological types, 476 with squamous cell carcinoma ( SCC ) , 361 with glandular cancer ( AC ) and 269 with other cell types viz. uniform malignant neoplastic disease, bronchioalveolar carcinoma and assorted cell carcinoma. It was supposed that SNP309 G allelomorph was interconnected with hazard of lung malignant neoplastic disease in all cell types compared to that of wild-type T allelomorph. In add-on, there was some grounds that SNP309 polymorphism had an association with other p53 polymorphism. Whether the patients had G/G genotype or p53 Arg72Pro polymorphism ( Pro/Pro genotype ) , there was a hazard of happening tumor and the hazard was even higher if the patients had both polymorphisms. However, there was no linkage between increased hazard of malignant neoplastic disease and Arg/Arg genotype because Arg/Arg genotype had more effectual apoptotic map and it could proficiently impede the transmutation of the cells. Besides, the cogent evidence for the interaction between smoking and SNP309 G allelomorph was important.

In add-on, the hazard of malignant neoplastic disease susceptibleness of non-small cell lung malignant neoplastic disease was well-studied with Norse population. Analysis for hazard of malignant neoplastic disease was higher in G allelomorph persons than those with T allelomorph and this consequence was even more outstanding in adult females because estrogen signalling has an impact on MDM2 look. This consequence of holding association between the hazard and SNP309 G allelomorph is equivalent to the hypothesis of Zhang et Al although the ethnics and histological cell types of tumor are wholly diverse.

Furthermore, in Korean population, the hazard of lung malignant neoplastic disease and SNP309 G allelomorph were besides correlated. Assorted histology types named SCC, AC, little cell carcinoma and big cell carcinoma were studied. The findings showed that the G allelomorph was seemingly connected with hazard of AC and later the more G allelomorph in patients, the greater the hazard of AC. However, in the determination of Zhang et Al, the hazard was equal in all different histological cell types.

Recent paper suggested that SNP309 G allelomorph and hazard of malignant neoplastic disease had no interconnectedness by utilizing two cultural groups, Afro-american and Caucasians. Besides, it was suggested that both gender and smoke were non associated with SNP309 polymorphism. Furthermore, the findings from one survey postulated that in Chinese patients, there was no associated consequence for SNP309 G allelomorph and hazard of malignant neoplastic disease. Interestingly, this consequence was inconsistent with the findings of Zhang et al whose experimental population was besides Chinese.

In contrast, SNP309 G allelomorph has been late identified as holding a protective consequence on the hazard of lung malignant neoplastic disease. It was studied with non-Hispanic white population and observed that wild-type T allelomorph caused increasing the hazard and the grounds for these contradictory consequences may be because of different tissue histology, cultural, familial background and familial susceptibleness of single patients to lung malignant neoplastic disease. Furthermore, the associated factors considered in each paper are besides non-identical.

Some research workers argued that SNP309 G allelomorph has no consequence on the hazard of malignant neoplastic diseases. The function of SNP309 polymorphism in respect to malignant neoplastic disease development becomes more flimsy than happening an reply. The fact that there was no correlativity between SNP309 polymorphism and the hazard of malignant neoplastic disease was proved by Pine et Al in African-American cultural. While Zheng et al stated the engagement of SNP309 G allelomorph in Chinese patients, another survey on Chinese malignant neoplastic disease patients by Hu et al proved otherwise. Whereas some surveies demonstrated that G allelomorph has a function in easing the development of malignant neoplastic diseases, others showed that G allelomorphs have a instead irregular protective consequence on the hazard of lung malignant neoplastic disease in comparing with wild-type T allelomorph. Due to the presence of different cultural groups, familial backgrounds and single susceptibleness to lung malignant neoplastic diseases being prevalent on each survey, they all account for diverse findings in respect to SNP309 polymorphism in lung malignant neoplastic disease hazard.

To sum up, SNP309 G allelomorph is predisposing the hazard of malignant neoplastic disease formation and its effects may be varied harmonizing to the histological subtypes. In add-on, it has interactive consequence on acceleration of malignant neoplastic disease with the p53 polymorphism. From crude cognition, smoke is a well-known carcinogens and it can do lung malignant neoplastic disease particularly in male. Yet, the estrogen receptor is participated in ordinance of MDM2 look and enhanced the fading of p53 tract. Therefore, the gender difference in lung malignant neoplastic disease may be.

HCC is one of the most prevalence malignant neoplastic diseases in Asian and major hazard factors are alcohol, aflatoxin, viral infection viz. hepatitis B virus ( HBV ) and hepatitis C virus ( HCV ) . Besides, some studies stated that the polymorphisms in the interleukin-1I? every bit good as UDP glucuronosyltransferase 1A7 cistrons take portion in the development of HCC. Therefore, research workers are funny to look into SNP309 polymorphism nowadays in the MDM2 cistron booster and its association of HCC.

In recent surveies, SNP309 G allelomorph was strongly modified the hazard of HCC patients who have underlying viral hepatitis infection. Experiment with 435 Nipponese patients who had chronic HCV infection revealed that the ratio of G allelomorph was higher than T allelomorph and G allelomorph had an influential consequence on hazard of doing HCC patients with HCV infection but non on the age of oncoming for tumor. In add-on, the relation between G allelomorph and intoxicant could non happen because the allele frequence was same whether the patients had cirrhosis or non. Therefore, the hypothesis can be drawn that SNP309 polymorphism is non strongly associated with cirrhosis in Nipponese and farther researches are required to infer a better confirmation.

Most of the surveies were consistent with each other and showed that SNP309 G allelomorph gave rise to acceleration of malignant neoplastic disease in patients with implicit in infection either HBV or HCV. Furthermore, one research paper proposed that there might be an association between G/G genotype SNP309 and p53 Arg72Pro polymorphism.

From these informations, we can reason that SNP309 G allele entirely may non excite HCC formation and it merely facilitates tumorigenesis with the 1s who have implicit in infection. Furthermore, most surveies of MDM2 polymorphism and HCC are done in Asiatic population so it is necessary to analyze in diverse population with big sample size to acquire better understanding the consequence of SBP309.

The sensitivity of SNP309 G allelomorph on oesophageal malignant neoplastic disease is besides funny to cognize and both environmental hazard factors and implicit in familial background drama a function in this tumorigenesis. The really first research paper was done with 758 Han Chinese patients and 1,420 control people, the consequences proposed that patients transporting G/G genotype had a higher hazard for the development of malignant neoplastic disease than T/T genotype bearers. However, the heterozygous bearers ( T/G ) were non associated with the hazard of malignant neoplastic disease so it could be assumed that G allelomorph has a recessionary consequence on this carcinogenesis. Furthermore, SNP309 polymorphism had a multiplicative consequence with p53 Arg72Pro polymorphism and with smoke every bit good. Among tobacco users, the uneven ratio was 2 to 3 times higher for those with both G/G and Pro/Pro genotypes than those with either one of them.

Overall, SNP309 G allelomorph may hold a predisposing consequence on carcinogenesis of gorge. Equally far as to this day of the month, Hong et al paper is the primordial and merely paper on analyzing the association between these two and many surveies on multiracial cultural with big sample size are extensively required to pull the decision.

Like other malignant neoplastic diseases, SNP309 polymorphism may be correlated with one of the hematologic upsets, leukemia, in term of incidence, oncoming of tumor, intervention result and forecast on incompatible ethnics. In acute lymphoblastic leukemia ( ALL ) patients, the impact of MDM2 polymorphism was varied harmonizing to the different populations. The earlier age of oncoming for variant G allelomorph could be noted in Caucasians and Black groups whereas in Latino population showed no difference.

Recently, in Chinese population, the G allelomorph could neither impact on the age of onset nor survival but even reduced the hazard of acute myeloid leukemia ( AML ) and acute lymphoid leukemia ( ALL ) which was incompatible with other consequences. Furthermore, G allele acted as a dominant allelomorph which means that either heterozygous ( T/G ) or homozygous ( G/G ) decreased the hazard in both male and female patients. Additionally, SNP309 G allelomorph did non hold cistron to cistron interaction with other p53 polymorphism in this tumor.

However, the association of this polymorphism and leukaemiogenesis could be observed neither for age of oncomings nor for incidence in B typed chronic lymphoblastic leukemia ( CLL ) though the obvious consequence of reduced overall endurance in patients was found. Yet in German society, SNP309 polymorphism had no sensitivity to both age of oncoming and result of CLL.

Therefore, in leukemia, the findings are unreconcilable with each other and the association with SNP309 may be conflicting due to different ethnics in each research and the gender prejudice can non be seen.

For stomachic malignant neoplastic disease, 410 Nipponese patients were extensively studied and found that the SNP309 G/G genotype was related with increased hazard for sporadic malignant neoplastic disease patients who had p53 mutant. G allelomorph had more prone to look excess stomachic tumor than T allelomorph but the age of tumour oncoming between these two allelomorphs was similar. This survey besides showed that the hapless forecast was concerned with SNP309 G/G genotype.

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