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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Fam Cancer. Author manuscript; available in PMC 2010 March 31.
Published in final edited form as:
PMCID: PMC2847875
NIHMSID: NIHMS187528

The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch Syndrome: from bench to bedside

Abstract

Lynch syndrome is an inherited disease caused by a germline mutation in one of four DNA mismatch repair (MMR) genes. The clinical manifestations can be somewhat variable depending upon which gene is involved, and where the mutation occurs. Moreover, the approach to the diagnosis of Lynch syndrome is becoming more complex as more is learned about the disease, and one needs to understand how the DNA MMR proteins function, and what makes them malfunction, to have an optimal appreciation of how to interpret diagnostic studies such as microsatellite instability and immunohistochemistry of the DNA MMR proteins. Finally, an understanding of the role of the DNA MMR system in regulation of the cell cycle and the response to DNA damage helps illuminate the differences in natural history and response to chemotherapeutic agents seen in Lynch syndrome.

Keywords: Lynch syndrome, HNPCC, DNA mismatch repair, Microsatellite instability, MSH2, MLH1, MSH6, PMS2, Colorectal cancer, Familial cancer

Introduction

Lynch syndrome is the hereditary disease caused by a germline mutation in one of four different human DNA mismatch repair (MMR) genes. This disease is inherited in an autosomal dominant fashion, and gives rise to familial clusters of cancers of the colon, endometrium, and other sites; the tumors have some characteristic pathological features and have an unusually early age of onset. With one exception (the Muir-Torre syndrome), there is no premorbid phenotype for this disease. However the tumors are best recognized by virtue of the unique mutational signature, microsatellite instability (MSI), that is present in the tumor tissue [1].

This review will focus upon the basic biology of defective DNA MMR, and provide correlation between the underlying mechanism of the disease and the clinical spectrum observed in Lynch syndrome. The defective DNA MMR activity is thought to be responsible for the unique phenotypic abnormalities seen in these tumors, including the more rapid adenoma-to-carcinoma transition, and the differential response to chemotherapy seen in this disease. Also, depending upon which of the DNA MMR genes is mutated, a slightly different clinical spectrum of disease may occur.

The DNA MMR system

The DNA MMR system consists of several nuclear proteins that act in concert to detect and repair errors that occur during the S phase of DNA replication. The critical elements of the DNA MMR system most relevant to Lynch syndrome are the MutS homologue (MSH) family and MutL homologue (MLH) family of proteins. As illustrated in Fig. 1, the MSH proteins always work as heterodimers. MSH2 is an obligatory partner in the system, and it may dimerize with either of two other family members: MSH6 or MSH3 [2]. The MSH2–MSH6 (MutSα) heterodimer preferentially recognizes and binds single base pair mismatches, such as the G-T mismatch illustrated in Fig. 1A, or mononucleotide repeats as shown in Fig. 1B. Through an energy-requiring process, free MutSα interacts with DNA at the site of a mismatch, exchanges ADP for ATP, and forms a sliding clamp around the DNA [3]. Alternatively, the MSH2-MSH3 pair (called MutSβ) preferentially recognizes larger “loop-out” errors, which can occur at dinucleotide repeats or other repetitive sequences.

Fig. 1
DNA MMR (A) Repair of a single nucleotide mismatch in S phase by MutSα. (MutL components not shown here) A. The polymerase has erroneously placed a G in the daughter strand across from a non-complementary T in the template, creating a mismatch. ...

MutS heterodimers signal the site of mispairing, however additional proteins are required to complete the repair process. The MutL family of proteins consists of one obligatory partner, MLH1, which may dimerize with PMS2, PMS1, or MLH3 (not shown in Fig. 1). Little is known about the MutL family beyond the function of the MLH1-PMS2 heterodimer, which is called MutLα. This heterodimer has endonuclease activity [4], interacts with the MutS-DNA complex, and together with ExoI, PCNA, and other enzymes required for DNA synthesis, the newly synthesized strand containing the error is excised, followed by resynthesis [5]. Repair of replication errors is required for the transition from S phase through G2 to mitosis [6].

Microsatellite Instability (MSI)

The absence of MSH2 or MLH1 leads to complete loss of DNA MMR activity. As a result, DNA synthetic errors accumulate at an accelerated rate as the cells proliferate. Therefore, tumor DNA from cancers with deficient DNA MMR activity has the characteristic mutational signature called MSI. As illustrated in Fig. 2, one can select a panel of five microsatellite sequences, amplify them by PCR, and compare these with the amplicons obtained at the same sequences in that individual's normal tissues [7]. In most instances, the mutations at the microsatellite sequences result in a deletion of one or more of the mononucleotide or dinucleotide elements, resulting in a shorter sequence. This can be detected when the PCR products are resolved by size using HPLC. A significant degree of MSI is called MSI-high (MSI-H), and is defined by the presence of mutations at two or more of the 5 consensus microsatellite sequences. Most CRCs have no mutated microsatellite sequences, so they are called “microsatellite stable” (MSS). Occasional tumors have only 1/5 ofthe microsatellites sequences mutated, and these are referred to as MSI-low, or MSI-L. Biologically, MSI-H cancers behave differently than those that are MSS or MSI-L, and subsequently in this review, MSI means MSI-H.

Fig. 2
Microsatellite Instability Five mononucleotide repeat sequences (NR21, BAT26, NR24, NR27, and BAT 25) were amplified in a multiplex reaction and separated by HPLC. The upper lanes labeled “normal DNA” represent DNA from lymphocytes, and ...

Target genes that mediate carcinogenesis in MSI tumors

It is thought that most of the mutations at the microsatellite sequences used to detect MSI in CRCs are not mechanistically responsible for the behavior of tumor cells. However, there are approximately 32 target genes in the human genome in which there is a mononucleotide repeat of seven or more elements (i.e., A10, G8, etc) in the coding sequence of the gene product [8]. The deletion of one of these elements leads to a frame shift, and loss of function of that gene. Longer repetitive elements are more prone to mutation than shorter ones.

The most commonly mutated gene in MSI-H tumors is the TGFβ1R2 gene, which contains an A10 sequence. This gene product is required for negative growth signaling through TGFβ-SMAD cascade. Most of the genes shown in Table 1 are either involved in the regulation of growth, the regulation of apoptosis, or are genes involved in DNA repair. Perhaps critical to the altered behavior of Lynch syndrome tumors, the BAX gene has a G8 sequence found in its coding region, and this sequence is mutated in approximately half of all tumors with MSI [9]. Curiously, each of the “minor” DNA MMR genes (i.e. MSH6, MSH3, MLH3, and PMS2) has a repetitive sequence of eight or more nucleotides in its coding sequence [10]. Furthermore, MSH2 has an encoded A7 sequence. Thus, once DNA MMR activity is reduced, other genes in the MMR family are prone to mutation at these repetitive sequences, leading to a progressive process in which the entire system can be inactivated [11]. Loss of DNA MMR activity greatly accelerates the rate of accumulation of mutations in genes responsible for restraining cell growth. This provides a reasonable hypothesis for the rapid growth of adenomas and transition to carcinoma seen in Lynch syndrome.

Table 1
Mutational targets in CRCs with MSI [8]

Cell models used to study human DNA MMR

Several cell models are available to study the underlying biology of defective DNA MMR in vitro. The HCT116 colon cancer cell line has biallelic mutations in the MLH1 gene. The HEC59 and LoVo colon cell lines both have biallelic mutations of the MSH2 gene. The DLD1 colon cancer cell line has mutations of the MSH6 gene. Furthermore, cell lines have been developed from these by stable chromosome transfer, which permits one to study the biology of these cells after restoration of DNA MMR activity. The HCT116+chr3 cell line has undergone a stable transfer of chromosome of 3 into the cells, which corrects the defect of MLH1 [12]. HEC59+chr2 and LoVo+chr2 cells have both had stable transfer of chromosome 2, which corrects the MSH2 defect [13, 14]. The HEC59 cell line has mutations in MSH2 and MSH6, and both are corrected by the stable transfer of chromosome 2 into this cell line.

Most CRCs with MSI are not caused by Lynch syndrome. A more common mechanism for loss of DNA MMR activity in CRC is epigenetic inactivation of the MLH1 gene by methylation of the promoter. The cell lines SW48 and RKO both have this defect, and these cells can be rendered DNA MMR proficient by the use of demethylating agents in vitro, which leads to re-expression of MLH1 in 24–48 h [15].

The use of these in vitro models has permitted us to observe the protein–protein interactions in the DNA MMR family, and provides insight into the biological features of defective DNA MMR activity. Figure 3 is a series of PCR gels and Western blots in which the upper panel (RT-PCR) represents the reverse transcriptase-PCR analyses of gene expression, and the lower panels demonstrate protein expression in these cells [16]. The cell line SW480 is a control CRC cell line with intact DNA MMR activity. As shown in the second lane from the left, HCT116 cells have a weak MLH1 band in the upper (RT-PCR) panel because of biallelic mutations in MLH1. The lower panel demonstrates no expression of MLH1 protein, illustrating the pathological nature of the mutation. Importantly, in spite of the robust presence of mRNA for the PMS2 gene in the upper panel, there is no corresponding PMS2 protein in the lower panel. Thus, mutational inactivation of MLH1 leads to destabilization of the PMS2 protein, presumably because of rapid turnover in the absence of a stabilizing protein binding partner. As shown in the third lane, restoration of MLH1 by stable transfer chromosome 3 leads to an increase in the RT-PCR band for MLH1, and the appearance of both MLH1 and PMS2 proteins in the lower panels.

Fig. 3
Analysis of mRNA and protein expression of the DNA MMR genes in CRC cell lines with mutations. The upper panel (labeled RT-PCR) with the dark background represents PCR gels. Each of the white bands is a PCR product. The lower panel (labeled Western blots) ...

The cell line LoVo has mutations in both alleles of MSH2, which leads to a complete loss of its mRNA, so there is no band in the upper RT-PCR panel. As shown in the lower panel, the loss of MSH2 protein leads to the loss of MSH2, MSH6, and MSH3 proteins, because the latter two require MSH2 for stabilization. The next lane illustrates DLD1, which has a missense mutation in the MSH6 gene. This mutation does not lead to loss of the mRNA; however there is complete loss of functional MSH6 protein. Because MSH6 is a “minor” MMR protein and plays no role in stabilizing other MutS proteins, its absence does not lead to the loss the other MutS proteins. MSH2 compensates for loss of MSH6 by binding to MSH3, as illustrated in the Western blots.

The cell line HCT15 (in the far right lane) is the parental line from which DLD1 was derived, and it shows the same molecular features as seen in DLD1. The cell line SW48 (in the 2nd lane from the right), has undergone methylation and silencing of the MLH1 gene. This leads to a total loss of the mRNA for MLH1, and a total loss of the proteins MLH1 and PMS2. Although not shown here, after demethylation of the MLH1 gene in vitro, both MLH1 and PMS2 are re-expressed.

Clinical implications of the biochemistry of human DNA MMR

Figure 3 demonstrated that MSH2 is required to stabilize both MSH6 and MSH3, but the reverse is not true. If MSH2 is absent, there is no DNA MMR activity. If either MSH6 or MSH3 is the only absent protein, some DNA MMR activity is preserved. Furthermore, whereas the absence of MSH2 will lead to the loss of all DNA MMR activity, isolated absence of MSH6 largely results in loss of single base mismatch repair. Thus, one may not see classical MSI in tumors associated with isolated MSH6 deficiency [1720], there may not be dinucleotide repeat instability, and one could be misled by the consensus panel of microsatellite markers (which uses three dinucleotide repeats and two mononucleotide repeats) [7]. Some of these tumors occasionally have only MSI-L [20].

On the basis of the underlying biology of interactions between DNA MMR proteins, one can explain some of the variable phenotypic spectrum seen in Lynch syndrome. First, germline mutations in the two major DNA MMR genes, MSH2 and MLH1, result in the “classic” form of Lynch syndrome. In both types of families, one sees typical MSI-H and the full spectrum of tumors. Germline mutations in the MSH6 gene lead to an attenuated form of Lynch syndrome with later onset of the tumors [20]. This is presumably because MSH3 dimerizes with MSH2, which permits partial DNA MMR activity, and delays the appearance of tumors.

Missense mutations in DNA MMR genes may lead to alterations in the enzymatic activity of the DNA MMR protein, but the protein may still persist in the cell. Although not shown in Fig. 3, certain missense mutations in MLH1 or MSH6 can lead to the translation of a non-functioning protein that will be detected by immunological techniques. Consequently, one may detect these proteins using immunohistochemistry (IHC), although the expression may be weak or heterogeneous in the cancer tissue. Missense mutations are especially common in MSH6, whereas deletions of the gene or premature stop codons are more common with MSH2.

For the reasons stated above, loss of MSH3 does not lead to total loss of DNA MMR activity. In spite of the fact that this gene is subject to somatic mutation in some MSI CRCs [21], no families with germline mutations in MSH3 have ever been reported, presumably because of the strong protective effects of the residual MutSα heterodimer (MSH2 + MSH6). In a similar fashion, germline mutations in the PMS2 gene lead to an attenuated form of the disease [2224]. This is presumably because MLH1 can also heterodimerize with MLH3 or PMS1, providing sufficient activity to compensate for the absence of the MutLα heterodimer (MLH1 + PMS2), and retard the onset of disease. Finally, although there have been individuals with mutations in MLH3 or ExoI 1 who have had colon cancers, there are no large, documented families with Lynch syndrome attributable to these genes [25].

Genotype and phenotype in lynch syndrome

In the context of the biochemical basis of DNA MMR, it becomes understandable why one expects a “classic” Lynch syndrome phenotype when the germline mutation occurs in one of the two “major” DNA mismatch repair genes—MSH2 or MLH1. When there are mutations in either of these genes, one sees high degrees of penetrance and classic family histories. The CRCs in these families almost always show MSI, and the offending gene can often be found using IHC. Some experience with DNA MMR IHC is required to avoid making errors in the interpretation.

MSH2

When there are germline mutations in MSH2, one usually sees no expression of MSH2 and MSH6 proteins at IHC of CRCs. Most of the mutations in MSH2 create premature stop codons, altered splice sites, or are large deletions or rearrangements within the gene, which completely abrogate gene expression. Deletions of exons 1–6 are particularly common, and large deletions may comprise up to one third of all of germline mutations in MSH2 [26].

MLH1

Lynch syndrome of the MLH1 type is somewhat more complicated. When MLH1 is lost by a genetic deletion or a premature stop codon, one sees loss of both MLH1 and PMS2 at IHC. Most of the CRCs show classic MSI, with rare exceptions (e.g., MLH1 D132H) [27]. However, the frequency of missense mutations is somewhat higher with MLH1 than in MSH2. Some of these will lead to a loss of the enzymatic activity of MLH1, but expression of the MLH1 and PMS2 proteins at IHC can be preserved, leading the pathologist to a falsely “negative” reading (i.e. the protein appears normal). A common scenario is to find weak or ambiguous MLH1 staining, and absent PMS2 staining; this is most likely to represent a germline missense mutation in MLH1. Since MLH1 is expressed in lower abundance than MSH2 [28], the staining is weaker and the pathologist will require some experience in the interpretation of these slides. Furthermore, DNA MMR protein expression is down-regulated in response to oxidative stress [29] and hypoxia [30], which further can confound the IHC with this protein.

The use of IHC for PMS2 may be useful in confusing cases of MLH1-type Lynch syndrome. As mentioned, if there is ambiguity in the interpretation of MLH1 expression, the loss of PMS2 is a useful confirmatory finding. Also, some mutations in MLH1 (specifically, missense mutations) may leave residual MLH1 expression at IHC, in spite of a total loss of MMR function. In these instances (which are uncommon), one sees MSI, and PMS2 expression is absent from the tumor, leading one to the proper diagnosis. Missense mutations in MLH1 can be difficult to interpret, and are more likely to be pathogenic when they occur in the interactive domains between MLH1 and PMS2, between the MutS and MutL heterodimers, or with ExoI, as shown in Fig. 4 [31]. Ultimately, one must consult an accurate data base for each sequence variation to determine which ones are pathogenic mutations and which are non-pathogenic polymorphisms. The proper interpretation may require either data from a large pedigree, or the use of in vitro functional analyses of the variant proteins [32].

Fig. 4
Interaction among the DNA MMR proteins. Each of the MutS homologues (MSH3, MSH6, and MSH2) interacts as a heterodimer with the MutL homologues (MLH1, PMS2, PMS1, and MLH3), acting as heterodimers, and the exonuclease, ExoI. Mutations that occur in the ...

The other major complicating feature of MLH1 IHC is the fact that about 15% of all CRCs show MSI, and most of this is due to the acquired silencing of the MLH1 gene due to promoter methylation [33]. About 75–80% of the CRCs which show MSI (i.e., 10–12% of all CRCs) develop MSI due to this acquired defect, and the other 20–25% (i.e., 3–4% of all CRCs) are due to Lynch syndrome. The acquired silencing of MLH1 usually occurs in older patients, but occasionally can be found younger ones.

MSH6

Lynch syndrome of the MSH6 type produces an attenuated phenotype, because of the partial compensation provided by the MSH3 protein. The cancers in patients with germline mutations in MSH6 tend to occur later in their lives; therefore, the term “attenuation” is a reference to age of onset, but not the eventual prevalence of cancer. However, by age 70, 71% of women with MSH6-type Lynch syndrome will have developed endometrial cancer [20]. Furthermore, CRCs are as penetrant in this disease as in the classic forms, but tend to occur later in life (mean age ~56 years) than in classic Lynch syndrome. Just as occurs with MLH1, some missense mutations in the MSH6 gene will increase the risk for cancer, but the tumors will still show staining of MSH6 protein at IHC.

PMS2

Lynch syndrome caused by germline mutations in PMS2 is the most challenging form of the disease. These mutations lead to an attenuated phenotype with weaker family histories and older ages of onset. However, there is some suggestion that germline mutations in PMS2 may be as common as those in MSH2 [23]. The tumors in PMS2-type Lynch syndrome will show MSI, and isolated loss of PMS2 staining at IHC. The diagnostic challenge is to distinguish this disease from certain missense mutations in MLH1 which lead to destabilization and isolated of the PMS2 protein at IHC [31]. The genetic diagnosis of this disease remains a great challenge because of the large number of pseudogenes which confound diagnostic DNA sequencing [34]. Unlike genetic testing for MSH2, MLH1, and MSH6, there are no commercially available tests for PMS2 at the time of this writing.

Clinical uses of MSI in CRC

Approximately 15% of all CRCs show MSI. There are three clinical uses of this information in CRC patients. The principal use of MSI testing is to find Lynch syndrome, as described above. Secondly, survival is significantly better in young patients with MSI (Fig. 5). This is not because these tumors are detected at earlier stages. Improved survival is found at all stages of disease. Importantly, patients with Stage I or II CRCs have five year survivals exceeding 90% [35]. The third clinical implication of MSI in CRC is the fact that these tumors do not have the same response to the administration of chemotherapy as do MSS (or MSI-L) tumors.

Fig. 5
Improved survival in young patients who have CRC with MSI. The ten year survival is significantly better for patients whose CRC tumors are MSI compared with those MSS. As illustrated, this is true for tumors detected at each of the stages. In each instance, ...

Our group demonstrated over a decade ago that CRC cell lines with defective DNA MMR are relatively resistant to the cytotoxic effects of several drugs, including alkylating agents and 5-fluorouracil [6, 36, 37]. In fact, DNA MMR-deficient tumors are broadly resistant to chemotherapeutic agents that damage DNA [38]. More importantly, one can restore sensitivity to these DNA-damaging agents by restoring DNA MMR activity, either through stable chromosome transfer, or by re-expression of the MLH1 gene after exposure to demethylating agents [15]. As shown in Fig. 6, one sees a significant difference in cloning efficiency for DNA MMR-deficient cell lines after exposure to either the alkylating agent MNNG [6] or 5-FU [39]. This was also observed using clonagenic assays after demethylating the MLH1 gene with 5-azacytidine [15]. This led to the suggestion that patients with MSI CRCs would see less benefit from treatment with 5-FU compared against patients with MSS CRCs.

Fig. 6
In vitro evidence for resistance to the alkylating agent MNNG by CRC cell lines with deficient DNA MMR activity. (A) The cell lines HCT116, HCT116+ch3M2, LoVo, and 2774 are all DNA MMR deficient, and have intact colony forming ability in the presence ...

Clinical confirmation of this has come from several groups, but the concept has not been free of controversy. Ribic et al. demonstrated in a retrospective study of patients who had been prospectively randomized into 5-FU-containing chemotherapeutic regimens that those with MSI CRCs failed to benefit from 5-FU. Moreover, there was a 2-fold, but not statistically significant, increase in mortality in these patients (Fig. 7) [40]. Similar findings have been reported by three other groups [37, 41, 42]. Thus, it is reasonable to exercise caution regarding chemotherapy in Lynch syndrome patients with Stage III, or especially Stage II, CRCs. It is possible that drugs will found in the future that will be selectively beneficial in this disease.

Fig. 7
Clinical outcomes in CRC patients treated with 5-FU adjuvant chemotherapy depends upon the DNA MMR status. (A) The upper panel shows survival in patients with Stage II or Stage III CRC not given adjuvant chemotherapy. The dotted line on the top cohort ...

Summary

In summary, the biochemistry of the DNA MMR system has been studied in a number of CRC cell lines, which has helped confirmed the predictions initially made in E. coli and in yeast. The human DNA MMR system is more complicated than that in lower organisms, in that all of the human DNA MMR proteins require heterodimerization to function, and selective losses of individual proteins has differential impact on the MMR system. This complexity in DNA MMR results in clinical heterogeneity among different families with Lynch syndrome. The role of DNA MMR in regulating the cell cycle and signaling apoptosis in response to DNA damage is of particular clinical importance, since these patients require additional consideration when planning possible cancer chemotherapy.

Contributor Information

C. Richard Boland, Department of Internal Medicine and Sammons Cancer Center, Baylor University Medical Center (250 Hoblitzelle), 3500 Gaston Avenue, Dallas, TX 75246, USA.

Minoru Koi, Department of Internal Medicine and Sammons Cancer Center, Baylor University Medical Center (250 Hoblitzelle), 3500 Gaston Avenue, Dallas, TX 75246, USA.

Dong K. Chang, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.

John M. Carethers, Department of Medicine, University of California, San Diego, CA, USA.

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